Canonical Allele Identifier: CA2114127

Gene: WNT10A

Linked Data

• dbSNP Id: rs754567070
• ExAC: 2:219757949 T / A
• gnomAD v2: 2-219757949-T-A
• gnomAD v4: 2-218893227-T-A
• MyVariant Identifiers: chr2:g.219757949T>A (hg19) ; chr2:g.218893227T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893227T>A , CM000664.2:g.218893227T>A	GRCh38
NC_000002.11:g.219757949T>A , CM000664.1:g.219757949T>A	GRCh37
NC_000002.10:g.219466193T>A	NCBI36
NG_012179.1:g.17695T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1210T>A MANE Select	ENSP00000258411.3:p.Cys404Ser
ENST00000258411.7:c.1210T>A	ENSP00000258411.3:p.Cys404Ser
ENST00000489887.1:n.7T>A
NM_025216.2:c.1210T>A	NP_079492.2:p.Cys404Ser
XM_011511928.1:c.1159T>A	XP_011510230.1:p.Cys387Ser
XM_011511929.1:c.1114T>A	XP_011510231.1:p.Cys372Ser
XM_011511930.1:c.830T>A	XP_011510232.1:p.Leu277Gln
XM_011511929.2:c.1114T>A	XP_011510231.1:p.Cys372Ser
NM_025216.3:c.1210T>A MANE Select	NP_079492.2:p.Cys404Ser