Canonical Allele Identifier: CA1955240406
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17642111_17642112delinsCT , CM000673.2:g.17642111_17642112delinsCT GRCh38
NC_000011.9:g.17663658_17663659delinsCT , CM000673.1:g.17663658_17663659delinsCT GRCh37
NC_000011.8:g.17620234_17620235delinsCT NCBI36
NG_033191.1:g.99739_99740delinsCT
NG_033191.2:g.99739_99740delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.8332-16_8332-15delinsCT ENSP00000382323.2:n.8332-16_8332-15delinsCT
ENST00000399397.6:c.8296-16_8296-15delinsCT MANE Select ENSP00000382329.2:n.8296-16_8296-15delinsCT
ENST00000399391.6:c.8332-16_8332-15delinsCT ENSP00000382323.2:n.8332-16_8332-15delinsCT
ENST00000399397.5:c.8296-16_8296-15delinsCT ENSP00000382329.2:n.8296-16_8296-15delinsCT
NM_001277269.1:c.8332-16_8332-15delinsCT NP_001264198.1:n.8332-16_8332-15delinsCT
NM_001292063.1:c.8296-16_8296-15delinsCT NP_001278992.1:n.8296-16_8296-15delinsCT
NM_001277269.2:c.8332-16_8332-15delinsCT NP_001264198.1:n.8332-16_8332-15delinsCT
NM_001292063.2:c.8296-16_8296-15delinsCT MANE Select NP_001278992.1:n.8296-16_8296-15delinsCT