Canonical Allele Identifier: CA1955232876
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17612307G= , CM000673.2:g.17612307G= GRCh38
NC_000011.9:g.17633854G= , CM000673.1:g.17633854G= GRCh37
NC_000011.8:g.17590430G= NCBI36
NG_033191.1:g.69935G=
NG_033191.2:g.69935G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.6305G= ENSP00000382323.2:p.Cys2102=
ENST00000399397.6:c.6269G= MANE Select ENSP00000382329.2:p.Cys2090=
ENST00000342528.2:c.3323G= ENSP00000341666.2:p.Cys1108=
ENST00000399391.6:c.6305G= ENSP00000382323.2:p.Cys2102=
ENST00000399397.5:c.6269G= ENSP00000382329.2:p.Cys2090=
NM_001277269.1:c.6305G= NP_001264198.1:p.Cys2102=
NM_001292063.1:c.6269G= NP_001278992.1:p.Cys2090=
NM_001277269.2:c.6305G= NP_001264198.1:p.Cys2102=
NM_001292063.2:c.6269G= MANE Select NP_001278992.1:p.Cys2090=