Canonical Allele Identifier: CA1328961571

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882295C= , CM000664.2:g.218882295C=	GRCh38
NC_000002.11:g.219747017C= , CM000664.1:g.219747017C=	GRCh37
NC_000002.10:g.219455261C=	NCBI36
NG_012179.1:g.6763C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.248C= MANE Select	ENSP00000258411.3:p.Ala83=
ENST00000258411.7:c.248C=	ENSP00000258411.3:p.Ala83=
ENST00000458582.1:c.135C=
NM_025216.2:c.248C=	NP_079492.2:p.Ala83=
XM_011511928.1:c.197C=	XP_011510230.1:p.Ala66=
XM_011511929.1:c.152C=	XP_011510231.1:p.Ala51=
XM_011511930.1:c.248C=	XP_011510232.1:p.Ala83=
XM_011511929.2:c.152C=	XP_011510231.1:p.Ala51=
NM_025216.3:c.248C= MANE Select	NP_079492.2:p.Ala83=