Canonical Allele Identifier: CA1328961338
Gene: WNT10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218881776C= , CM000664.2:g.218881776C= GRCh38
NC_000002.11:g.219746498C= , CM000664.1:g.219746498C= GRCh37
NC_000002.10:g.219454742C= NCBI36
NG_012179.1:g.6244C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.114-385C= MANE Select ENSP00000258411.3:n.114-385C=
ENST00000258411.7:c.114-385C= ENSP00000258411.3:n.114-385C=
NM_025216.2:c.114-385C= NP_079492.2:n.114-385C=
XM_011511928.1:c.62+309C= XP_011510230.1:n.62+309C=
XM_011511929.1:c.18-385C= XP_011510231.1:n.18-385C=
XM_011511930.1:c.114-385C= XP_011510232.1:n.114-385C=
XM_011511929.2:c.18-385C= XP_011510231.1:n.18-385C=
NM_025216.3:c.114-385C= MANE Select NP_079492.2:n.114-385C=