Canonical Allele Identifier: CA1328961362

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218881837C= , CM000664.2:g.218881837C=	GRCh38
NC_000002.11:g.219746559C= , CM000664.1:g.219746559C=	GRCh37
NC_000002.10:g.219454803C=	NCBI36
NG_012179.1:g.6305C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.114-324C= MANE Select	ENSP00000258411.3:n.114-324C=
ENST00000258411.7:c.114-324C=	ENSP00000258411.3:n.114-324C=
NM_025216.2:c.114-324C=	NP_079492.2:n.114-324C=
XM_011511928.1:c.63-324C=	XP_011510230.1:n.63-324C=
XM_011511929.1:c.18-324C=	XP_011510231.1:n.18-324C=
XM_011511930.1:c.114-324C=	XP_011510232.1:n.114-324C=
XM_011511929.2:c.18-324C=	XP_011510231.1:n.18-324C=
NM_025216.3:c.114-324C= MANE Select	NP_079492.2:n.114-324C=