Canonical Allele Identifier: CA1328961567

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882281C= , CM000664.2:g.218882281C=	GRCh38
NC_000002.11:g.219747003C= , CM000664.1:g.219747003C=	GRCh37
NC_000002.10:g.219455247C=	NCBI36
NG_012179.1:g.6749C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.234C= MANE Select	ENSP00000258411.3:p.His78=
ENST00000258411.7:c.234C=	ENSP00000258411.3:p.His78=
ENST00000458582.1:c.121C=
NM_025216.2:c.234C=	NP_079492.2:p.His78=
XM_011511928.1:c.183C=	XP_011510230.1:p.His61=
XM_011511929.1:c.138C=	XP_011510231.1:p.His46=
XM_011511930.1:c.234C=	XP_011510232.1:p.His78=
XM_011511929.2:c.138C=	XP_011510231.1:p.His46=
NM_025216.3:c.234C= MANE Select	NP_079492.2:p.His78=