Canonical Allele Identifier: CA2790598502
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17635179_17635181del , CM000673.2:g.17635179_17635181del GRCh38
NC_000011.9:g.17656726_17656728del , CM000673.1:g.17656726_17656728del GRCh37
NC_000011.8:g.17613302_17613304del NCBI36
NG_033191.1:g.92807_92809del
NG_033191.2:g.92807_92809del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.7721_7723del ENSP00000382323.2:p.Tyr2574del
ENST00000399397.6:c.7685_7687del MANE Select ENSP00000382329.2:p.Tyr2562del
ENST00000342528.2:c.4322-431_4322-429del ENSP00000341666.2:n.4322-431_4322-429del
ENST00000399391.6:c.7721_7723del ENSP00000382323.2:p.Tyr2574del
ENST00000399397.5:c.7685_7687del ENSP00000382329.2:p.Tyr2562del
NM_001277269.1:c.7721_7723del NP_001264198.1:p.Tyr2574del
NM_001292063.1:c.7685_7687del NP_001278992.1:p.Tyr2562del
NM_001277269.2:c.7721_7723del NP_001264198.1:p.Tyr2574del
NM_001292063.2:c.7685_7687del MANE Select NP_001278992.1:p.Tyr2562del