Canonical Allele Identifier: CA2838982836
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553427dup , CM000673.2:g.17553427dup GRCh38
NC_000011.9:g.17574974dup , CM000673.1:g.17574974dup GRCh37
NC_000011.8:g.17531550dup NCBI36
NG_033191.1:g.11055dup
NG_033191.2:g.11055dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.484dup ENSP00000382323.2:p.Thr162AsnfsTer3
ENST00000399397.6:c.448dup MANE Select ENSP00000382329.2:p.Thr150AsnfsTer3
ENST00000399391.6:c.484dup ENSP00000382323.2:p.Thr162AsnfsTer3
ENST00000399397.5:c.448dup ENSP00000382329.2:p.Thr150AsnfsTer3
ENST00000428619.1:c.265dup ENSP00000399057.2:p.Thr89AsnfsTer3
ENST00000498332.5:n.354dup
NM_001277269.1:c.484dup NP_001264198.1:p.Thr162AsnfsTer3
NM_001292063.1:c.448dup NP_001278992.1:p.Thr150AsnfsTer3
NM_001277269.2:c.484dup NP_001264198.1:p.Thr162AsnfsTer3
NM_001292063.2:c.448dup MANE Select NP_001278992.1:p.Thr150AsnfsTer3