Canonical Allele Identifier: CA350592161

Gene: WNT10A

Linked Data

• dbSNP Id: rs1397288018
• gnomAD v3: 2-218893183-G-A
• gnomAD v4: 2-218893183-G-A
• MyVariant Identifiers: chr2:g.219757905G>A (hg19) ; chr2:g.218893183G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893183G>A , CM000664.2:g.218893183G>A	GRCh38
NC_000002.11:g.219757905G>A , CM000664.1:g.219757905G>A	GRCh37
NC_000002.10:g.219466149G>A	NCBI36
NG_012179.1:g.17651G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1166G>A MANE Select	ENSP00000258411.3:p.Ser389Asn
ENST00000258411.7:c.1166G>A	ENSP00000258411.3:p.Ser389Asn
NM_025216.2:c.1166G>A	NP_079492.2:p.Ser389Asn
XM_011511928.1:c.1115G>A	XP_011510230.1:p.Ser372Asn
XM_011511929.1:c.1070G>A	XP_011510231.1:p.Ser357Asn
XM_011511930.1:c.786G>A	XP_011510232.1:p.Gln262=
XM_011511929.2:c.1070G>A	XP_011510231.1:p.Ser357Asn
NM_025216.3:c.1166G>A MANE Select	NP_079492.2:p.Ser389Asn