Canonical Allele Identifier: CA1955232883
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17612319G= , CM000673.2:g.17612319G= GRCh38
NC_000011.9:g.17633866G= , CM000673.1:g.17633866G= GRCh37
NC_000011.8:g.17590442G= NCBI36
NG_033191.1:g.69947G=
NG_033191.2:g.69947G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.6317G= ENSP00000382323.2:p.Trp2106=
ENST00000399397.6:c.6281G= MANE Select ENSP00000382329.2:p.Trp2094=
ENST00000342528.2:c.3335G= ENSP00000341666.2:p.Trp1112=
ENST00000399391.6:c.6317G= ENSP00000382323.2:p.Trp2106=
ENST00000399397.5:c.6281G= ENSP00000382329.2:p.Trp2094=
NM_001277269.1:c.6317G= NP_001264198.1:p.Trp2106=
NM_001292063.1:c.6281G= NP_001278992.1:p.Trp2094=
NM_001277269.2:c.6317G= NP_001264198.1:p.Trp2106=
NM_001292063.2:c.6281G= MANE Select NP_001278992.1:p.Trp2094=