Canonical Allele Identifier: CA2574770026
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553310del , CM000673.2:g.17553310del GRCh38
NC_000011.9:g.17574857del , CM000673.1:g.17574857del GRCh37
NC_000011.8:g.17531433del NCBI36
NG_033191.1:g.10938del
NG_033191.2:g.10938del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.422-55del ENSP00000382323.2:n.422-55del
ENST00000399397.6:c.386-55del MANE Select ENSP00000382329.2:n.386-55del
ENST00000399391.6:c.422-55del ENSP00000382323.2:n.422-55del
ENST00000399397.5:c.386-55del ENSP00000382329.2:n.386-55del
ENST00000428619.1:c.203-55del ENSP00000399057.2:n.203-55del
ENST00000498332.5:n.292-55del
NM_001277269.1:c.422-55del NP_001264198.1:n.422-55del
NM_001292063.1:c.386-55del NP_001278992.1:n.386-55del
NM_001277269.2:c.422-55del NP_001264198.1:n.422-55del
NM_001292063.2:c.386-55del MANE Select NP_001278992.1:n.386-55del