Canonical Allele Identifier: CA431234838

Gene: WNT10A

Linked Data

• dbSNP Id: rs1447019141
• gnomAD v2: 2-219757930-C-T
• gnomAD v4: 2-218893208-C-T
• MyVariant Identifiers: chr2:g.219757930C>T (hg19) ; chr2:g.218893208C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893208C>T , CM000664.2:g.218893208C>T	GRCh38
NC_000002.11:g.219757930C>T , CM000664.1:g.219757930C>T	GRCh37
NC_000002.10:g.219466174C>T	NCBI36
NG_012179.1:g.17676C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1191C>T MANE Select	ENSP00000258411.3:p.His397=
ENST00000258411.7:c.1191C>T	ENSP00000258411.3:p.His397=
NM_025216.2:c.1191C>T	NP_079492.2:p.His397=
XM_011511928.1:c.1140C>T	XP_011510230.1:p.His380=
XM_011511929.1:c.1095C>T	XP_011510231.1:p.His365=
XM_011511930.1:c.811C>T	XP_011510232.1:p.Leu271=
XM_011511929.2:c.1095C>T	XP_011510231.1:p.His365=
NM_025216.3:c.1191C>T MANE Select	NP_079492.2:p.His397=