Canonical Allele Identifier: CA431234843

Gene: WNT10A

Linked Data

• ClinVar Variation Id: 2943208
• ClinVar RCV Id: RCV003800326
• MyVariant Identifiers: chr2:g.219757945G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893223G>C , CM000664.2:g.218893223G>C	GRCh38
NC_000002.11:g.219757945G>C , CM000664.1:g.219757945G>C	GRCh37
NC_000002.10:g.219466189G>C	NCBI36
NG_012179.1:g.17691G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1206G>C MANE Select	ENSP00000258411.3:p.Val402=
ENST00000258411.7:c.1206G>C	ENSP00000258411.3:p.Val402=
ENST00000489887.1:n.3G>C
NM_025216.2:c.1206G>C	NP_079492.2:p.Val402=
XM_011511928.1:c.1155G>C	XP_011510230.1:p.Val385=
XM_011511929.1:c.1110G>C	XP_011510231.1:p.Val370=
XM_011511930.1:c.826G>C	XP_011510232.1:p.Gly276Arg
XM_011511929.2:c.1110G>C	XP_011510231.1:p.Val370=
NM_025216.3:c.1206G>C MANE Select	NP_079492.2:p.Val402=