Canonical Allele Identifier: CA539621550
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs1433162229

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218881723_218881726del , CM000664.2:g.218881723_218881726del GRCh38
NC_000002.11:g.219746445_219746448del , CM000664.1:g.219746445_219746448del GRCh37
NC_000002.10:g.219454689_219454692del NCBI36
NG_012179.1:g.6191_6194del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.114-438_114-435del MANE Select ENSP00000258411.3:n.114-438_114-435del
ENST00000258411.7:c.114-438_114-435del ENSP00000258411.3:n.114-438_114-435del
NM_025216.2:c.114-438_114-435del NP_079492.2:n.114-438_114-435del
XM_011511928.1:c.62+256_62+259del XP_011510230.1:n.62+256_62+259del
XM_011511929.1:c.18-438_18-435del XP_011510231.1:n.18-438_18-435del
XM_011511930.1:c.114-438_114-435del XP_011510232.1:n.114-438_114-435del
XM_011511929.2:c.18-438_18-435del XP_011510231.1:n.18-438_18-435del
NM_025216.3:c.114-438_114-435del MANE Select NP_079492.2:n.114-438_114-435del