Canonical Allele Identifier: CA218489773
Gene: OTOG HGNC NCBI

Linked Data

dbSNP Id: rs553174068

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553145G>A , CM000673.2:g.17553145G>A GRCh38
NC_000011.9:g.17574692G>A , CM000673.1:g.17574692G>A GRCh37
NC_000011.8:g.17531268G>A NCBI36
NG_033191.1:g.10773G>A
NG_033191.2:g.10773G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.355G>A ENSP00000382323.2:p.Glu119Lys
ENST00000399397.6:c.319G>A MANE Select ENSP00000382329.2:p.Glu107Lys
ENST00000399391.6:c.355G>A ENSP00000382323.2:p.Glu119Lys
ENST00000399397.5:c.319G>A ENSP00000382329.2:p.Glu107Lys
ENST00000428619.1:c.136G>A ENSP00000399057.2:p.Glu46Lys
ENST00000498332.5:n.225G>A
NM_001277269.1:c.355G>A NP_001264198.1:p.Glu119Lys
NM_001292063.1:c.319G>A NP_001278992.1:p.Glu107Lys
NM_001277269.2:c.355G>A NP_001264198.1:p.Glu119Lys
NM_001292063.2:c.319G>A MANE Select NP_001278992.1:p.Glu107Lys