Canonical Allele Identifier: CA1328965688

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893273C= , CM000664.2:g.218893273C=	GRCh38
NC_000002.11:g.219757995C= , CM000664.1:g.219757995C=	GRCh37
NC_000002.10:g.219466239C=	NCBI36
NG_012179.1:g.17741C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000258411.8:c.*2C= MANE Select	ENSP00000258411.3:n.*2C=
ENST00000258411.7:c.*2C=	ENSP00000258411.3:n.*2C=
ENST00000489887.1:n.47+6C=
NM_025216.2:c.*2C=	NP_079492.2:n.*2C=
XM_011511928.1:c.*2C=	XP_011510230.1:n.*2C=
XM_011511929.1:c.*2C=	XP_011510231.1:n.*2C=
XM_011511930.1:c.876C=	XP_011510232.1:p.Ser292=
XM_011511929.2:c.*2C=	XP_011510231.1:n.*2C=
NM_025216.3:c.*2C= MANE Select	NP_079492.2:n.*2C=