Canonical Allele Identifier: CA1328961519

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882186C= , CM000664.2:g.218882186C=	GRCh38
NC_000002.11:g.219746908C= , CM000664.1:g.219746908C=	GRCh37
NC_000002.10:g.219455152C=	NCBI36
NG_012179.1:g.6654C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.139C= MANE Select	ENSP00000258411.3:p.Leu47=
ENST00000258411.7:c.139C=	ENSP00000258411.3:p.Leu47=
ENST00000458582.1:c.26C=
NM_025216.2:c.139C=	NP_079492.2:p.Leu47=
XM_011511928.1:c.88C=	XP_011510230.1:p.Leu30=
XM_011511929.1:c.43C=	XP_011510231.1:p.Leu15=
XM_011511930.1:c.139C=	XP_011510232.1:p.Leu47=
XM_011511929.2:c.43C=	XP_011510231.1:p.Leu15=
NM_025216.3:c.139C= MANE Select	NP_079492.2:p.Leu47=