Canonical Allele Identifier: CA1955197799
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553490G= , CM000673.2:g.17553490G= GRCh38
NC_000011.9:g.17575037G= , CM000673.1:g.17575037G= GRCh37
NC_000011.8:g.17531613G= NCBI36
NG_033191.1:g.11118G=
NG_033191.2:g.11118G=

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.547G= ENSP00000382323.2:p.Glu183=
ENST00000399397.6:c.511G= MANE Select ENSP00000382329.2:p.Glu171=
ENST00000399391.6:c.547G= ENSP00000382323.2:p.Glu183=
ENST00000399397.5:c.511G= ENSP00000382329.2:p.Glu171=
ENST00000498332.5:n.417G=
NM_001277269.1:c.547G= NP_001264198.1:p.Glu183=
NM_001292063.1:c.511G= NP_001278992.1:p.Glu171=
NM_001277269.2:c.547G= NP_001264198.1:p.Glu183=
NM_001292063.2:c.511G= MANE Select NP_001278992.1:p.Glu171=