Canonical Allele Identifier: CA346468022

Gene: ALK

Linked Data

• dbSNP Id: rs2148178661
• MyVariant Identifiers: chr2:g.29449914T>A (hg19) ; chr2:g.29227048T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29227048T>A , CM000664.2:g.29227048T>A	GRCh38
NC_000002.11:g.29449914T>A , CM000664.1:g.29449914T>A	GRCh37
NC_000002.10:g.29303418T>A	NCBI36
NG_009445.1:g.699519A>T , LRG_488:g.699519A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.2941A>T MANE Select	ENSP00000373700.3:p.Ile981Phe
ENST00000431873.6:c.107A>T
ENST00000389048.7:c.2941A>T	ENSP00000373700.3:p.Ile981Phe
ENST00000618119.4:c.1810A>T	ENSP00000482733.1:p.Ile604Phe
NM_004304.4:c.2941A>T	NP_004295.2:p.Ile981Phe
XM_024452778.1:c.94A>T	XP_024308546.1:p.Ile32Phe
XR_001738688.2:n.3797A>T
NM_004304.5:c.2941A>T MANE Select	NP_004295.2:p.Ile981Phe