Canonical Allele Identifier: CA379811093
Gene: OTOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553380C>A , CM000673.2:g.17553380C>A GRCh38
NC_000011.9:g.17574927C>A , CM000673.1:g.17574927C>A GRCh37
NC_000011.8:g.17531503C>A NCBI36
NG_033191.1:g.11008C>A
NG_033191.2:g.11008C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.437C>A ENSP00000382323.2:p.Pro146His
ENST00000399397.6:c.401C>A MANE Select ENSP00000382329.2:p.Pro134His
ENST00000399391.6:c.437C>A ENSP00000382323.2:p.Pro146His
ENST00000399397.5:c.401C>A ENSP00000382329.2:p.Pro134His
ENST00000428619.1:c.218C>A ENSP00000399057.2:p.Pro73His
ENST00000498332.5:n.307C>A
NM_001277269.1:c.437C>A NP_001264198.1:p.Pro146His
NM_001292063.1:c.401C>A NP_001278992.1:p.Pro134His
NM_001277269.2:c.437C>A NP_001264198.1:p.Pro146His
NM_001292063.2:c.401C>A MANE Select NP_001278992.1:p.Pro134His