Canonical Allele Identifier: CA1955197739
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553374C= , CM000673.2:g.17553374C= GRCh38
NC_000011.9:g.17574921C= , CM000673.1:g.17574921C= GRCh37
NC_000011.8:g.17531497C= NCBI36
NG_033191.1:g.11002C=
NG_033191.2:g.11002C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.431C= ENSP00000382323.2:p.Ala144=
ENST00000399397.6:c.395C= MANE Select ENSP00000382329.2:p.Ala132=
ENST00000399391.6:c.431C= ENSP00000382323.2:p.Ala144=
ENST00000399397.5:c.395C= ENSP00000382329.2:p.Ala132=
ENST00000428619.1:c.212C= ENSP00000399057.2:p.Ala71=
ENST00000498332.5:n.301C=
NM_001277269.1:c.431C= NP_001264198.1:p.Ala144=
NM_001292063.1:c.395C= NP_001278992.1:p.Ala132=
NM_001277269.2:c.431C= NP_001264198.1:p.Ala144=
NM_001292063.2:c.395C= MANE Select NP_001278992.1:p.Ala132=