Canonical Allele Identifier: CA350618425

Gene: WNT10A

Linked Data

• MyVariant Identifiers: chr2:g.219746966G>A (hg19) ; chr2:g.218882244G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882244G>A , CM000664.2:g.218882244G>A	GRCh38
NC_000002.11:g.219746966G>A , CM000664.1:g.219746966G>A	GRCh37
NC_000002.10:g.219455210G>A	NCBI36
NG_012179.1:g.6712G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.197G>A MANE Select	ENSP00000258411.3:p.Gly66Asp
ENST00000258411.7:c.197G>A	ENSP00000258411.3:p.Gly66Asp
ENST00000458582.1:c.84G>A
NM_025216.2:c.197G>A	NP_079492.2:p.Gly66Asp
XM_011511928.1:c.146G>A	XP_011510230.1:p.Gly49Asp
XM_011511929.1:c.101G>A	XP_011510231.1:p.Gly34Asp
XM_011511930.1:c.197G>A	XP_011510232.1:p.Gly66Asp
XM_011511929.2:c.101G>A	XP_011510231.1:p.Gly34Asp
NM_025216.3:c.197G>A MANE Select	NP_079492.2:p.Gly66Asp