Canonical Allele Identifier: CA346474209
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 2443128
ClinVar RCV Id: RCV003151520 RCV003633681
COSMIC: COSM4398113
MyVariant Identifiers: chr2:g.29551258G>A (hg19) chr2:g.29328392G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328392G>A , CM000664.2:g.29328392G>A GRCh38
NC_000002.11:g.29551258G>A , CM000664.1:g.29551258G>A GRCh37
NC_000002.10:g.29404762G>A NCBI36
NG_009445.1:g.598175C>T , LRG_488:g.598175C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000389048.8:c.1372C>T MANE Select ENSP00000373700.3:p.His458Tyr
ENST00000389048.7:c.1372C>T ENSP00000373700.3:p.His458Tyr
ENST00000618119.4:c.241C>T ENSP00000482733.1:p.His81Tyr
NM_004304.4:c.1372C>T NP_004295.2:p.His458Tyr
XR_939920.1:n.700G>A
XR_939921.1:n.680+5864G>A
XR_001738688.2:n.2302C>T
XR_939920.2:n.590G>A
XR_939921.2:n.576+5864G>A
NM_004304.5:c.1372C>T MANE Select NP_004295.2:p.His458Tyr
Search 100 bp 5'
Search 100 bp 3'