Canonical Allele Identifier: CA346474232

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29551263T>A (hg19) ; chr2:g.29328397T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29328397T>A , CM000664.2:g.29328397T>A	GRCh38
NC_000002.11:g.29551263T>A , CM000664.1:g.29551263T>A	GRCh37
NC_000002.10:g.29404767T>A	NCBI36
NG_009445.1:g.598170A>T , LRG_488:g.598170A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.1367A>T MANE Select	ENSP00000373700.3:p.Asp456Val
ENST00000389048.7:c.1367A>T	ENSP00000373700.3:p.Asp456Val
ENST00000618119.4:c.236A>T	ENSP00000482733.1:p.Asp79Val
NM_004304.4:c.1367A>T	NP_004295.2:p.Asp456Val
XR_939920.1:n.705T>A
XR_939921.1:n.680+5869T>A
XR_001738688.2:n.2297A>T
XR_939920.2:n.595T>A
XR_939921.2:n.576+5869T>A
NM_004304.5:c.1367A>T MANE Select	NP_004295.2:p.Asp456Val