Canonical Allele Identifier: CA346468115
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 1519392
ClinVar RCV Id: RCV002024577 RCV003382817
dbSNP Id: rs1472378906
gnomAD v4: 2-29227065-C-A
MyVariant Identifiers: chr2:g.29449931C>A (hg19) chr2:g.29227065C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29227065C>A , CM000664.2:g.29227065C>A GRCh38
NC_000002.11:g.29449931C>A , CM000664.1:g.29449931C>A GRCh37
NC_000002.10:g.29303435C>A NCBI36
NG_009445.1:g.699502G>T , LRG_488:g.699502G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.2924G>T MANE Select ENSP00000373700.3:p.Gly975Val
ENST00000431873.6:c.90G>T
ENST00000389048.7:c.2924G>T ENSP00000373700.3:p.Gly975Val
ENST00000618119.4:c.1793G>T ENSP00000482733.1:p.Gly598Val
NM_004304.4:c.2924G>T NP_004295.2:p.Gly975Val
XM_024452778.1:c.77G>T XP_024308546.1:p.Gly26Val
XR_001738688.2:n.3780G>T
NM_004304.5:c.2924G>T MANE Select NP_004295.2:p.Gly975Val
Search 100 bp 5'
Search 100 bp 3'