Varaico: Literature-Extracted Genetic Variants

Gene:ALK
Variant:p.L1256F
Back to variants list

ALK

NM_004304.5:p.L1256F

Associated Papers

Sustained Complete Response to Brigatinib in a Young Patient With ALK-Positive NSCLC Harboring I1171N Mutation Post-Alectinib Resistance.

Kapoor A et al.

Case Reports in Oncological Medicine, 2026

Discriminating activating, deactivating and resistance variants in protein kinases.

Singh G et al.

Genome Medicine, 2025

41152984 (PubMed )
Supplement: 13073_2025_1564_MOESM2_ESM.xlsx › Table_S6

Discovery of an ALK degrader for lorlatinib-resistant compound mutations.

Gao F et al.

European Journal of Medicinal Chemistry, 2025

Prediction of potential drug-resistant ALK mutations against fourth-generation inhibitors NVL-655 and TPX-0131.

Zhao F et al.

International Journal of Biological Macromolecules, 2025

ALK-tyrosine kinase inhibitor intrinsic resistance due to de novo MET-amplification in metastatic ALK-rearranged non-small cell lung cancer effectively treated by alectinib-crizotinib combination-case report.

Urbanska EM et al.

Translational Lung Cancer Research, 2024

TKI type switching overcomes ROS1 L2086F in ROS1 fusion-positive cancers.

Thawani R et al.

Npj Precision Oncology, 2024

TKI Type Switching Overcomes ROS1 L2086F in ROS1 Fusion-Positive Cancers.

Thawani R et al.

Biorxiv : the Preprint Server for Biology, 2024

Overcoming Central β-Sheet #6 (Cβ6) ALK Mutation (L1256F), TP53 Mutations and Short Forms of EML4-ALK v3/b and v5a/b Splice Variants are the Unmet Need That a Re-Imagined 5th-Generation (5G) ALK TKI Must Deliver.

Lee ATM et al.

Lung Cancer (auckland, N.z.), 2024

EML4-ALK biology and drug resistance in non-small cell lung cancer: a new phase of discoveries.

Elshatlawy M et al.

Molecular Oncology, 2023

Deciphering the Shared and Specific Drug Resistance Mechanisms of Anaplastic Lymphoma Kinase via Binding Free Energy Computation.

Yu Y et al.

Research (washington, D.c.), 2023

Anaplastic lymphoma kinase inhibitors-a review of anticancer properties, clinical efficacy, and resistance mechanisms.

Kiełbowski K et al.

Frontiers in Pharmacology, 2023

Case report: SAF-189s is a potent inhibitor in a lorlatinib-resistant NSCLC patient with acquired compound mutations ALK L1196M and D1203N.

Li N et al.

Frontiers in Pharmacology, 2023

The return of RET GateKeeper mutations? an in-silico exploratory analysis of potential resistance mechanisms to novel RET macrocyclic inhibitor TPX-0046.

Repetto M et al.

Investigational New Drugs, 2022

Crizotinib-Resistant ROS1 G2101A Mutation Associated With Sensitivity to Lorlatinib in ROS1-Rearranged NSCLC: Case Report.

Begum P et al.

Jto Clinical and Research Reports, 2022

Will the clinical development of 4th-generation "double mutant active" ALK TKIs (TPX-0131 and NVL-655) change the future treatment paradigm of ALK+ NSCLC?

Ou SI et al.

Translational Oncology, 2021

Spectrum of Mechanisms of Resistance to Crizotinib and Lorlatinib in ROS1 Fusion-Positive Lung Cancer.

Lin JJ et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2021

Gilteritinib overcomes lorlatinib resistance in ALK-rearranged cancer.

Mizuta H et al.

Nature Communications, 2021

A Novel Sequentially Evolved EML4-ALK Variant 3 G1202R/S1206Y Double Mutation In Cis Confers Resistance to Lorlatinib: A Brief Report and Literature Review.

Zhu VW et al.

Jto Clinical and Research Reports, 2021

Overcoming resistance by ALK compound mutation (I1171S + G1269A) after sequential treatment of multiple ALK inhibitors in non-small cell lung cancer.

Takahashi K et al.

Thoracic Cancer, 2020

Prediction of ALK mutations mediating ALK-TKIs resistance and drug re-purposing to overcome the resistance.

Okada K et al.

Ebiomedicine, 2019

EIF2AK4 mutations in pulmonary capillary hemangiomatosis.

Best DH et al.

Chest, 2014

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."