Canonical Allele Identifier: CA5905355
Gene: OTOG HGNC NCBI

Linked Data

dbSNP Id: rs766987353

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553384G>A , CM000673.2:g.17553384G>A GRCh38
NC_000011.9:g.17574931G>A , CM000673.1:g.17574931G>A GRCh37
NC_000011.8:g.17531507G>A NCBI36
NG_033191.1:g.11012G>A
NG_033191.2:g.11012G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.441G>A ENSP00000382323.2:p.Glu147=
ENST00000399397.6:c.405G>A MANE Select ENSP00000382329.2:p.Glu135=
ENST00000399391.6:c.441G>A ENSP00000382323.2:p.Glu147=
ENST00000399397.5:c.405G>A ENSP00000382329.2:p.Glu135=
ENST00000428619.1:c.222G>A ENSP00000399057.2:p.Glu74=
ENST00000498332.5:n.311G>A
NM_001277269.1:c.441G>A NP_001264198.1:p.Glu147=
NM_001292063.1:c.405G>A NP_001278992.1:p.Glu135=
NM_001277269.2:c.441G>A NP_001264198.1:p.Glu147=
NM_001292063.2:c.405G>A MANE Select NP_001278992.1:p.Glu135=