Canonical Allele Identifier: CA1328965654

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893248G= , CM000664.2:g.218893248G=	GRCh38
NC_000002.11:g.219757970G= , CM000664.1:g.219757970G=	GRCh37
NC_000002.10:g.219466214G=	NCBI36
NG_012179.1:g.17716G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1231G= MANE Select	ENSP00000258411.3:p.Glu411=
ENST00000258411.7:c.1231G=	ENSP00000258411.3:p.Glu411=
ENST00000489887.1:n.28G=
NM_025216.2:c.1231G=	NP_079492.2:p.Glu411=
XM_011511928.1:c.1180G=	XP_011510230.1:p.Glu394=
XM_011511929.1:c.1135G=	XP_011510231.1:p.Glu379=
XM_011511930.1:c.851G=	XP_011510232.1:p.Arg284=
XM_011511929.2:c.1135G=	XP_011510231.1:p.Glu379=
NM_025216.3:c.1231G= MANE Select	NP_079492.2:p.Glu411=