Canonical Allele Identifier: CA65849735
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs528604165

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218881680_218881681del , CM000664.2:g.218881680_218881681del GRCh38
NC_000002.11:g.219746402_219746403del , CM000664.1:g.219746402_219746403del GRCh37
NC_000002.10:g.219454646_219454647del NCBI36
NG_012179.1:g.6148_6149del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.114-481_114-480del MANE Select ENSP00000258411.3:n.114-481_114-480del
ENST00000258411.7:c.114-481_114-480del ENSP00000258411.3:n.114-481_114-480del
NM_025216.2:c.114-481_114-480del NP_079492.2:n.114-481_114-480del
XM_011511928.1:c.62+213_62+214del XP_011510230.1:n.62+213_62+214del
XM_011511929.1:c.18-481_18-480del XP_011510231.1:n.18-481_18-480del
XM_011511930.1:c.114-481_114-480del XP_011510232.1:n.114-481_114-480del
XM_011511929.2:c.18-481_18-480del XP_011510231.1:n.18-481_18-480del
NM_025216.3:c.114-481_114-480del MANE Select NP_079492.2:n.114-481_114-480del