Canonical Allele Identifier: CA1328965581

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893195A= , CM000664.2:g.218893195A=	GRCh38
NC_000002.11:g.219757917A= , CM000664.1:g.219757917A=	GRCh37
NC_000002.10:g.219466161A=	NCBI36
NG_012179.1:g.17663A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1178A= MANE Select	ENSP00000258411.3:p.His393=
ENST00000258411.7:c.1178A=	ENSP00000258411.3:p.His393=
NM_025216.2:c.1178A=	NP_079492.2:p.His393=
XM_011511928.1:c.1127A=	XP_011510230.1:p.His376=
XM_011511929.1:c.1082A=	XP_011510231.1:p.His361=
XM_011511930.1:c.798A=	XP_011510232.1:p.Pro266=
XM_011511929.2:c.1082A=	XP_011510231.1:p.His361=
NM_025216.3:c.1178A= MANE Select	NP_079492.2:p.His393=