Canonical Allele Identifier: CA1328965721

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893292C= , CM000664.2:g.218893292C=	GRCh38
NC_000002.11:g.219758014C= , CM000664.1:g.219758014C=	GRCh37
NC_000002.10:g.219466258C=	NCBI36
NG_012179.1:g.17760C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.*21C= MANE Select	ENSP00000258411.3:n.*21C=
ENST00000258411.7:c.*21C=	ENSP00000258411.3:n.*21C=
ENST00000489887.1:n.47+25C=
NM_025216.2:c.*21C=	NP_079492.2:n.*21C=
XM_011511928.1:c.*21C=	XP_011510230.1:n.*21C=
XM_011511929.1:c.*21C=	XP_011510231.1:n.*21C=
XM_011511930.1:c.895C=	XP_011510232.1:p.Pro299=
XM_011511929.2:c.*21C=	XP_011510231.1:n.*21C=
NM_025216.3:c.*21C= MANE Select	NP_079492.2:n.*21C=