Canonical Allele Identifier: CA425434664

Gene: ALK

Linked Data

• dbSNP Id: rs2148155189
• MyVariant Identifiers: chr2:g.29432693C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29209827C>A , CM000664.2:g.29209827C>A	GRCh38
NC_000002.11:g.29432693C>A , CM000664.1:g.29432693C>A	GRCh37
NC_000002.10:g.29286197C>A	NCBI36
NG_009445.1:g.716740G>T , LRG_488:g.716740G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3795G>T MANE Select	ENSP00000373700.3:p.Val1265=
ENST00000431873.6:c.1022G>T
ENST00000638605.1:n.672G>T
ENST00000642122.1:c.591G>T	ENSP00000493203.1:p.Val197=
ENST00000389048.7:c.3795G>T	ENSP00000373700.3:p.Val1265=
ENST00000431873.5:c.675G>T	ENSP00000414027.2:p.Val225=
ENST00000618119.4:c.2664G>T	ENSP00000482733.1:p.Val888=
NM_004304.4:c.3795G>T	NP_004295.2:p.Val1265=
NM_001353765.1:c.591G>T	NP_001340694.1:p.Val197=
XM_024452778.1:c.948G>T	XP_024308546.1:p.Val316=
XM_024452779.1:c.591G>T	XP_024308547.1:p.Val197=
NM_004304.5:c.3795G>T MANE Select	NP_004295.2:p.Val1265=
NM_001353765.2:c.591G>T	NP_001340694.1:p.Val197=