Canonical Allele Identifier: CA1328961562

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882267G= , CM000664.2:g.218882267G=	GRCh38
NC_000002.11:g.219746989G= , CM000664.1:g.219746989G=	GRCh37
NC_000002.10:g.219455233G=	NCBI36
NG_012179.1:g.6735G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.220G= MANE Select	ENSP00000258411.3:p.Val74=
ENST00000258411.7:c.220G=	ENSP00000258411.3:p.Val74=
ENST00000458582.1:c.107G=
NM_025216.2:c.220G=	NP_079492.2:p.Val74=
XM_011511928.1:c.169G=	XP_011510230.1:p.Val57=
XM_011511929.1:c.124G=	XP_011510231.1:p.Val42=
XM_011511930.1:c.220G=	XP_011510232.1:p.Val74=
XM_011511929.2:c.124G=	XP_011510231.1:p.Val42=
NM_025216.3:c.220G= MANE Select	NP_079492.2:p.Val74=