Canonical Allele Identifier: CA346473095

Gene: ALK

Linked Data

• dbSNP Id: rs2148166573
• MyVariant Identifiers: chr2:g.29443652A>C (hg19) ; chr2:g.29220786A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220786A>C , CM000664.2:g.29220786A>C	GRCh38
NC_000002.11:g.29443652A>C , CM000664.1:g.29443652A>C	GRCh37
NC_000002.10:g.29297156A>C	NCBI36
NG_009445.1:g.705781T>G , LRG_488:g.705781T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.3565T>G MANE Select	ENSP00000373700.3:p.Ser1189Ala
ENST00000431873.6:c.792T>G
ENST00000638605.1:n.442T>G
ENST00000642122.1:c.361T>G	ENSP00000493203.1:p.Ser121Ala
ENST00000389048.7:c.3565T>G	ENSP00000373700.3:p.Ser1189Ala
ENST00000431873.5:c.445T>G	ENSP00000414027.2:p.Ser149Ala
ENST00000618119.4:c.2434T>G	ENSP00000482733.1:p.Ser812Ala
NM_004304.4:c.3565T>G	NP_004295.2:p.Ser1189Ala
NM_001353765.1:c.361T>G	NP_001340694.1:p.Ser121Ala
XM_024452778.1:c.718T>G	XP_024308546.1:p.Ser240Ala
XM_024452779.1:c.361T>G	XP_024308547.1:p.Ser121Ala
NM_004304.5:c.3565T>G MANE Select	NP_004295.2:p.Ser1189Ala
NM_001353765.2:c.361T>G	NP_001340694.1:p.Ser121Ala