Canonical Allele Identifier: CA425434665

Gene: ALK

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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