Canonical Allele Identifier: CA431416407

Gene: WNT10A

Linked Data

• MyVariant Identifiers: chr2:g.219746904G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882182G>C , CM000664.2:g.218882182G>C	GRCh38
NC_000002.11:g.219746904G>C , CM000664.1:g.219746904G>C	GRCh37
NC_000002.10:g.219455148G>C	NCBI36
NG_012179.1:g.6650G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.135G>C MANE Select	ENSP00000258411.3:p.Leu45=
ENST00000258411.7:c.135G>C	ENSP00000258411.3:p.Leu45=
ENST00000458582.1:c.22G>C
NM_025216.2:c.135G>C	NP_079492.2:p.Leu45=
XM_011511928.1:c.84G>C	XP_011510230.1:p.Leu28=
XM_011511929.1:c.39G>C	XP_011510231.1:p.Leu13=
XM_011511930.1:c.135G>C	XP_011510232.1:p.Leu45=
XM_011511929.2:c.39G>C	XP_011510231.1:p.Leu13=
NM_025216.3:c.135G>C MANE Select	NP_079492.2:p.Leu45=