Canonical Allele Identifier: CA1328961569

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882289T= , CM000664.2:g.218882289T=	GRCh38
NC_000002.11:g.219747011T= , CM000664.1:g.219747011T=	GRCh37
NC_000002.10:g.219455255T=	NCBI36
NG_012179.1:g.6757T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.242T= MANE Select	ENSP00000258411.3:p.Val81=
ENST00000258411.7:c.242T=	ENSP00000258411.3:p.Val81=
ENST00000458582.1:c.129T=
NM_025216.2:c.242T=	NP_079492.2:p.Val81=
XM_011511928.1:c.191T=	XP_011510230.1:p.Val64=
XM_011511929.1:c.146T=	XP_011510231.1:p.Val49=
XM_011511930.1:c.242T=	XP_011510232.1:p.Val81=
XM_011511929.2:c.146T=	XP_011510231.1:p.Val49=
NM_025216.3:c.242T= MANE Select	NP_079492.2:p.Val81=