Canonical Allele Identifier: CA1328965828

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893412G= , CM000664.2:g.218893412G=	GRCh38
NC_000002.11:g.219758134G= , CM000664.1:g.219758134G=	GRCh37
NC_000002.10:g.219466378G=	NCBI36
NG_012179.1:g.17880G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.*141G= MANE Select	ENSP00000258411.3:n.*141G=
ENST00000258411.7:c.*141G=	ENSP00000258411.3:n.*141G=
ENST00000489887.1:n.47+145G=
NM_025216.2:c.*141G=	NP_079492.2:n.*141G=
XM_011511928.1:c.*141G=	XP_011510230.1:n.*141G=
XM_011511929.1:c.*141G=	XP_011510231.1:n.*141G=
XM_011511930.1:c.*115G=	XP_011510232.1:n.*115G=
XM_011511929.2:c.*141G=	XP_011510231.1:n.*141G=
NM_025216.3:c.*141G= MANE Select	NP_079492.2:n.*141G=