Canonical Allele Identifier: CA431416799

Gene: WNT10A

Linked Data

• dbSNP Id: rs1244920095
• gnomAD v2: 2-219754986-C-A
• COSMIC: COSM4741389
• MyVariant Identifiers: chr2:g.219754986C>A (hg19) ; chr2:g.218890264C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218890264C>A , CM000664.2:g.218890264C>A	GRCh38
NC_000002.11:g.219754986C>A , CM000664.1:g.219754986C>A	GRCh37
NC_000002.10:g.219463230C>A	NCBI36
NG_012179.1:g.14732C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000258411.8:c.657C>A MANE Select	ENSP00000258411.3:p.Gly219=
ENST00000258411.7:c.657C>A	ENSP00000258411.3:p.Gly219=
ENST00000458582.1:c.264-2510C>A
NM_025216.2:c.657C>A	NP_079492.2:p.Gly219=
XM_011511928.1:c.606C>A	XP_011510230.1:p.Gly202=
XM_011511929.1:c.561C>A	XP_011510231.1:p.Gly187=
XM_011511930.1:c.377-2510C>A	XP_011510232.1:n.377-2510C>A
XM_011511929.2:c.561C>A	XP_011510231.1:p.Gly187=
NM_025216.3:c.657C>A MANE Select	NP_079492.2:p.Gly219=