Canonical Allele Identifier: CA1955236969
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17635171C= , CM000673.2:g.17635171C= GRCh38
NC_000011.9:g.17656718C= , CM000673.1:g.17656718C= GRCh37
NC_000011.8:g.17613294C= NCBI36
NG_033191.1:g.92799C=
NG_033191.2:g.92799C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.7713C= ENSP00000382323.2:p.Cys2571=
ENST00000399397.6:c.7677C= MANE Select ENSP00000382329.2:p.Cys2559=
ENST00000342528.2:c.4322-439C= ENSP00000341666.2:n.4322-439C=
ENST00000399391.6:c.7713C= ENSP00000382323.2:p.Cys2571=
ENST00000399397.5:c.7677C= ENSP00000382329.2:p.Cys2559=
NM_001277269.1:c.7713C= NP_001264198.1:p.Cys2571=
NM_001292063.1:c.7677C= NP_001278992.1:p.Cys2559=
NM_001277269.2:c.7713C= NP_001264198.1:p.Cys2571=
NM_001292063.2:c.7677C= MANE Select NP_001278992.1:p.Cys2559=