Canonical Allele Identifier: CA425434662

Gene: ALK

Linked Data

• ClinVar Variation Id: 470846
• ClinVar RCV Id: RCV000542294
• dbSNP Id: rs1553391502
• MyVariant Identifiers: chr2:g.29432690G>T (hg19) ; chr2:g.29209824G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29209824G>T , CM000664.2:g.29209824G>T	GRCh38
NC_000002.11:g.29432690G>T , CM000664.1:g.29432690G>T	GRCh37
NC_000002.10:g.29286194G>T	NCBI36
NG_009445.1:g.716743C>A , LRG_488:g.716743C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3798C>A MANE Select	ENSP00000373700.3:p.Ala1266=
ENST00000431873.6:c.1025C>A
ENST00000638605.1:n.675C>A
ENST00000642122.1:c.594C>A	ENSP00000493203.1:p.Ala198=
ENST00000389048.7:c.3798C>A	ENSP00000373700.3:p.Ala1266=
ENST00000431873.5:c.678C>A	ENSP00000414027.2:p.Ala226=
ENST00000618119.4:c.2667C>A	ENSP00000482733.1:p.Ala889=
NM_004304.4:c.3798C>A	NP_004295.2:p.Ala1266=
NM_001353765.1:c.594C>A	NP_001340694.1:p.Ala198=
XM_024452778.1:c.951C>A	XP_024308546.1:p.Ala317=
XM_024452779.1:c.594C>A	XP_024308547.1:p.Ala198=
NM_004304.5:c.3798C>A MANE Select	NP_004295.2:p.Ala1266=
NM_001353765.2:c.594C>A	NP_001340694.1:p.Ala198=