Canonical Allele Identifier: CA425435991

Gene: ALK

Linked Data

• dbSNP Id: rs2148178556
• MyVariant Identifiers: chr2:g.29449879T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29227013T>A , CM000664.2:g.29227013T>A	GRCh38
NC_000002.11:g.29449879T>A , CM000664.1:g.29449879T>A	GRCh37
NC_000002.10:g.29303383T>A	NCBI36
NG_009445.1:g.699554A>T , LRG_488:g.699554A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.2976A>T MANE Select	ENSP00000373700.3:p.Val992=
ENST00000431873.6:c.142A>T
ENST00000389048.7:c.2976A>T	ENSP00000373700.3:p.Val992=
ENST00000618119.4:c.1845A>T	ENSP00000482733.1:p.Val615=
NM_004304.4:c.2976A>T	NP_004295.2:p.Val992=
XM_024452778.1:c.129A>T	XP_024308546.1:p.Val43=
XR_001738688.2:n.3832A>T
NM_004304.5:c.2976A>T MANE Select	NP_004295.2:p.Val992=