Canonical Allele Identifier: CA1328961543

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882237T= , CM000664.2:g.218882237T=	GRCh38
NC_000002.11:g.219746959T= , CM000664.1:g.219746959T=	GRCh37
NC_000002.10:g.219455203T=	NCBI36
NG_012179.1:g.6705T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.190T= MANE Select	ENSP00000258411.3:p.Leu64=
ENST00000258411.7:c.190T=	ENSP00000258411.3:p.Leu64=
ENST00000458582.1:c.77T=
NM_025216.2:c.190T=	NP_079492.2:p.Leu64=
XM_011511928.1:c.139T=	XP_011510230.1:p.Leu47=
XM_011511929.1:c.94T=	XP_011510231.1:p.Leu32=
XM_011511930.1:c.190T=	XP_011510232.1:p.Leu64=
XM_011511929.2:c.94T=	XP_011510231.1:p.Leu32=
NM_025216.3:c.190T= MANE Select	NP_079492.2:p.Leu64=