Canonical Allele Identifier: CA346467732

Gene: ALK

Linked Data

• dbSNP Id: rs2148178526
• MyVariant Identifiers: chr2:g.29449871C>A (hg19) ; chr2:g.29227005C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29227005C>A , CM000664.2:g.29227005C>A	GRCh38
NC_000002.11:g.29449871C>A , CM000664.1:g.29449871C>A	GRCh37
NC_000002.10:g.29303375C>A	NCBI36
NG_009445.1:g.699562G>T , LRG_488:g.699562G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.2984G>T MANE Select	ENSP00000373700.3:p.Cys995Phe
ENST00000431873.6:c.150G>T
ENST00000389048.7:c.2984G>T	ENSP00000373700.3:p.Cys995Phe
ENST00000618119.4:c.1853G>T	ENSP00000482733.1:p.Cys618Phe
NM_004304.4:c.2984G>T	NP_004295.2:p.Cys995Phe
XM_024452778.1:c.137G>T	XP_024308546.1:p.Cys46Phe
XR_001738688.2:n.3840G>T
NM_004304.5:c.2984G>T MANE Select	NP_004295.2:p.Cys995Phe