Canonical Allele Identifier: CA431416450

Gene: WNT10A

Linked Data

• MyVariant Identifiers: chr2:g.219746964A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882242A>C , CM000664.2:g.218882242A>C	GRCh38
NC_000002.11:g.219746964A>C , CM000664.1:g.219746964A>C	GRCh37
NC_000002.10:g.219455208A>C	NCBI36
NG_012179.1:g.6710A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.195A>C MANE Select	ENSP00000258411.3:p.Pro65=
ENST00000258411.7:c.195A>C	ENSP00000258411.3:p.Pro65=
ENST00000458582.1:c.82A>C
NM_025216.2:c.195A>C	NP_079492.2:p.Pro65=
XM_011511928.1:c.144A>C	XP_011510230.1:p.Pro48=
XM_011511929.1:c.99A>C	XP_011510231.1:p.Pro33=
XM_011511930.1:c.195A>C	XP_011510232.1:p.Pro65=
XM_011511929.2:c.99A>C	XP_011510231.1:p.Pro33=
NM_025216.3:c.195A>C MANE Select	NP_079492.2:p.Pro65=