Canonical Allele Identifier: CA1328965593

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893201G= , CM000664.2:g.218893201G=	GRCh38
NC_000002.11:g.219757923G= , CM000664.1:g.219757923G=	GRCh37
NC_000002.10:g.219466167G=	NCBI36
NG_012179.1:g.17669G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1184G= MANE Select	ENSP00000258411.3:p.Arg395=
ENST00000258411.7:c.1184G=	ENSP00000258411.3:p.Arg395=
NM_025216.2:c.1184G=	NP_079492.2:p.Arg395=
XM_011511928.1:c.1133G=	XP_011510230.1:p.Arg378=
XM_011511929.1:c.1088G=	XP_011510231.1:p.Arg363=
XM_011511930.1:c.804G=	XP_011510232.1:p.Pro268=
XM_011511929.2:c.1088G=	XP_011510231.1:p.Arg363=
NM_025216.3:c.1184G= MANE Select	NP_079492.2:p.Arg395=