Canonical Allele Identifier: CA1328965626

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893220C= , CM000664.2:g.218893220C=	GRCh38
NC_000002.11:g.219757942C= , CM000664.1:g.219757942C=	GRCh37
NC_000002.10:g.219466186C=	NCBI36
NG_012179.1:g.17688C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1203C= MANE Select	ENSP00000258411.3:p.Phe401=
ENST00000258411.7:c.1203C=	ENSP00000258411.3:p.Phe401=
NM_025216.2:c.1203C=	NP_079492.2:p.Phe401=
XM_011511928.1:c.1152C=	XP_011510230.1:p.Phe384=
XM_011511929.1:c.1107C=	XP_011510231.1:p.Phe369=
XM_011511930.1:c.823C=	XP_011510232.1:p.Arg275=
XM_011511929.2:c.1107C=	XP_011510231.1:p.Phe369=
NM_025216.3:c.1203C= MANE Select	NP_079492.2:p.Phe401=