Canonical Allele Identifier: CA346468136

Gene: ALK

Linked Data

• dbSNP Id: rs2148178722
• MyVariant Identifiers: chr2:g.29449935C>T (hg19) ; chr2:g.29227069C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29227069C>T , CM000664.2:g.29227069C>T	GRCh38
NC_000002.11:g.29449935C>T , CM000664.1:g.29449935C>T	GRCh37
NC_000002.10:g.29303439C>T	NCBI36
NG_009445.1:g.699498G>A , LRG_488:g.699498G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.2920G>A MANE Select	ENSP00000373700.3:p.Glu974Lys
ENST00000431873.6:c.86G>A
ENST00000389048.7:c.2920G>A	ENSP00000373700.3:p.Glu974Lys
ENST00000618119.4:c.1789G>A	ENSP00000482733.1:p.Glu597Lys
NM_004304.4:c.2920G>A	NP_004295.2:p.Glu974Lys
XM_024452778.1:c.73G>A	XP_024308546.1:p.Glu25Lys
XR_001738688.2:n.3776G>A
NM_004304.5:c.2920G>A MANE Select	NP_004295.2:p.Glu974Lys