Canonical Allele Identifier: CA1955233050
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17612621C= , CM000673.2:g.17612621C= GRCh38
NC_000011.9:g.17634168C= , CM000673.1:g.17634168C= GRCh37
NC_000011.8:g.17590744C= NCBI36
NG_033191.1:g.70249C=
NG_033191.2:g.70249C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.6330C= ENSP00000382323.2:p.Cys2110=
ENST00000399397.6:c.6294C= MANE Select ENSP00000382329.2:p.Cys2098=
ENST00000342528.2:c.3348C= ENSP00000341666.2:p.Cys1116=
ENST00000399391.6:c.6330C= ENSP00000382323.2:p.Cys2110=
ENST00000399397.5:c.6294C= ENSP00000382329.2:p.Cys2098=
NM_001277269.1:c.6330C= NP_001264198.1:p.Cys2110=
NM_001292063.1:c.6294C= NP_001278992.1:p.Cys2098=
NM_001277269.2:c.6330C= NP_001264198.1:p.Cys2110=
NM_001292063.2:c.6294C= MANE Select NP_001278992.1:p.Cys2098=