Canonical Allele Identifier: CA379811114
Gene: OTOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553383A>T , CM000673.2:g.17553383A>T GRCh38
NC_000011.9:g.17574930A>T , CM000673.1:g.17574930A>T GRCh37
NC_000011.8:g.17531506A>T NCBI36
NG_033191.1:g.11011A>T
NG_033191.2:g.11011A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.440A>T ENSP00000382323.2:p.Glu147Val
ENST00000399397.6:c.404A>T MANE Select ENSP00000382329.2:p.Glu135Val
ENST00000399391.6:c.440A>T ENSP00000382323.2:p.Glu147Val
ENST00000399397.5:c.404A>T ENSP00000382329.2:p.Glu135Val
ENST00000428619.1:c.221A>T ENSP00000399057.2:p.Glu74Val
ENST00000498332.5:n.310A>T
NM_001277269.1:c.440A>T NP_001264198.1:p.Glu147Val
NM_001292063.1:c.404A>T NP_001278992.1:p.Glu135Val
NM_001277269.2:c.440A>T NP_001264198.1:p.Glu147Val
NM_001292063.2:c.404A>T MANE Select NP_001278992.1:p.Glu135Val