Canonical Allele Identifier: CA350592840

Gene: WNT10A

Linked Data

• dbSNP Id: rs1944679690
• gnomAD v4: 2-218893260-G-A
• MyVariant Identifiers: chr2:g.219757982G>A (hg19) ; chr2:g.218893260G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893260G>A , CM000664.2:g.218893260G>A	GRCh38
NC_000002.11:g.219757982G>A , CM000664.1:g.219757982G>A	GRCh37
NC_000002.10:g.219466226G>A	NCBI36
NG_012179.1:g.17728G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1243G>A MANE Select	ENSP00000258411.3:p.Val415Ile
ENST00000258411.7:c.1243G>A	ENSP00000258411.3:p.Val415Ile
ENST00000489887.1:n.40G>A
NM_025216.2:c.1243G>A	NP_079492.2:p.Val415Ile
XM_011511928.1:c.1192G>A	XP_011510230.1:p.Val398Ile
XM_011511929.1:c.1147G>A	XP_011510231.1:p.Val383Ile
XM_011511930.1:c.863G>A	XP_011510232.1:p.Arg288His
XM_011511929.2:c.1147G>A	XP_011510231.1:p.Val383Ile
NM_025216.3:c.1243G>A MANE Select	NP_079492.2:p.Val415Ile