Canonical Allele Identifier: CA346467909

Gene: ALK

Linked Data

• dbSNP Id: rs2148178608
• MyVariant Identifiers: chr2:g.29449895C>A (hg19) ; chr2:g.29227029C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29227029C>A , CM000664.2:g.29227029C>A	GRCh38
NC_000002.11:g.29449895C>A , CM000664.1:g.29449895C>A	GRCh37
NC_000002.10:g.29303399C>A	NCBI36
NG_009445.1:g.699538G>T , LRG_488:g.699538G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.2960G>T MANE Select	ENSP00000373700.3:p.Cys987Phe
ENST00000431873.6:c.126G>T
ENST00000389048.7:c.2960G>T	ENSP00000373700.3:p.Cys987Phe
ENST00000618119.4:c.1829G>T	ENSP00000482733.1:p.Cys610Phe
NM_004304.4:c.2960G>T	NP_004295.2:p.Cys987Phe
XM_024452778.1:c.113G>T	XP_024308546.1:p.Cys38Phe
XR_001738688.2:n.3816G>T
NM_004304.5:c.2960G>T MANE Select	NP_004295.2:p.Cys987Phe