Canonical Allele Identifier: CA431416462

Gene: WNT10A

Linked Data

• ClinVar Variation Id: 2932532
• ClinVar RCV Id: RCV003795746
• MyVariant Identifiers: chr2:g.219746977C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882255C>A , CM000664.2:g.218882255C>A	GRCh38
NC_000002.11:g.219746977C>A , CM000664.1:g.219746977C>A	GRCh37
NC_000002.10:g.219455221C>A	NCBI36
NG_012179.1:g.6723C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.208C>A MANE Select	ENSP00000258411.3:p.Arg70=
ENST00000258411.7:c.208C>A	ENSP00000258411.3:p.Arg70=
ENST00000458582.1:c.95C>A
NM_025216.2:c.208C>A	NP_079492.2:p.Arg70=
XM_011511928.1:c.157C>A	XP_011510230.1:p.Arg53=
XM_011511929.1:c.112C>A	XP_011510231.1:p.Arg38=
XM_011511930.1:c.208C>A	XP_011510232.1:p.Arg70=
XM_011511929.2:c.112C>A	XP_011510231.1:p.Arg38=
NM_025216.3:c.208C>A MANE Select	NP_079492.2:p.Arg70=