Canonical Allele Identifier: CA350618606

Gene: WNT10A

Linked Data

• dbSNP Id: rs748131786
• MyVariant Identifiers: chr2:g.219746998C>A (hg19) ; chr2:g.218882276C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882276C>A , CM000664.2:g.218882276C>A	GRCh38
NC_000002.11:g.219746998C>A , CM000664.1:g.219746998C>A	GRCh37
NC_000002.10:g.219455242C>A	NCBI36
NG_012179.1:g.6744C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.229C>A MANE Select	ENSP00000258411.3:p.Arg77Ser
ENST00000258411.7:c.229C>A	ENSP00000258411.3:p.Arg77Ser
ENST00000458582.1:c.116C>A
NM_025216.2:c.229C>A	NP_079492.2:p.Arg77Ser
XM_011511928.1:c.178C>A	XP_011510230.1:p.Arg60Ser
XM_011511929.1:c.133C>A	XP_011510231.1:p.Arg45Ser
XM_011511930.1:c.229C>A	XP_011510232.1:p.Arg77Ser
XM_011511929.2:c.133C>A	XP_011510231.1:p.Arg45Ser
NM_025216.3:c.229C>A MANE Select	NP_079492.2:p.Arg77Ser