Canonical Allele Identifier: CA1328961310
Gene: WNT10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218881710_218881712delinsGTC , CM000664.2:g.218881710_218881712delinsGTC GRCh38
NC_000002.11:g.219746432_219746434delinsGTC , CM000664.1:g.219746432_219746434delinsGTC GRCh37
NC_000002.10:g.219454676_219454678delinsGTC NCBI36
NG_012179.1:g.6178_6180delinsGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.114-451_114-449delinsGTC MANE Select ENSP00000258411.3:n.114-451_114-449delinsGTC
ENST00000258411.7:c.114-451_114-449delinsGTC ENSP00000258411.3:n.114-451_114-449delinsGTC
NM_025216.2:c.114-451_114-449delinsGTC NP_079492.2:n.114-451_114-449delinsGTC
XM_011511928.1:c.62+243_62+245delinsGTC XP_011510230.1:n.62+243_62+245delinsGTC
XM_011511929.1:c.18-451_18-449delinsGTC XP_011510231.1:n.18-451_18-449delinsGTC
XM_011511930.1:c.114-451_114-449delinsGTC XP_011510232.1:n.114-451_114-449delinsGTC
XM_011511929.2:c.18-451_18-449delinsGTC XP_011510231.1:n.18-451_18-449delinsGTC
NM_025216.3:c.114-451_114-449delinsGTC MANE Select NP_079492.2:n.114-451_114-449delinsGTC