Canonical Allele Identifier: CA1328961358

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218881833T= , CM000664.2:g.218881833T=	GRCh38
NC_000002.11:g.219746555T= , CM000664.1:g.219746555T=	GRCh37
NC_000002.10:g.219454799T=	NCBI36
NG_012179.1:g.6301T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.114-328T= MANE Select	ENSP00000258411.3:n.114-328T=
ENST00000258411.7:c.114-328T=	ENSP00000258411.3:n.114-328T=
NM_025216.2:c.114-328T=	NP_079492.2:n.114-328T=
XM_011511928.1:c.63-328T=	XP_011510230.1:n.63-328T=
XM_011511929.1:c.18-328T=	XP_011510231.1:n.18-328T=
XM_011511930.1:c.114-328T=	XP_011510232.1:n.114-328T=
XM_011511929.2:c.18-328T=	XP_011510231.1:n.18-328T=
NM_025216.3:c.114-328T= MANE Select	NP_079492.2:n.114-328T=