Canonical Allele Identifier: CA1955197782
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553463G= , CM000673.2:g.17553463G= GRCh38
NC_000011.9:g.17575010G= , CM000673.1:g.17575010G= GRCh37
NC_000011.8:g.17531586G= NCBI36
NG_033191.1:g.11091G=
NG_033191.2:g.11091G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.520G= ENSP00000382323.2:p.Gly174=
ENST00000399397.6:c.484G= MANE Select ENSP00000382329.2:p.Gly162=
ENST00000399391.6:c.520G= ENSP00000382323.2:p.Gly174=
ENST00000399397.5:c.484G= ENSP00000382329.2:p.Gly162=
ENST00000498332.5:n.390G=
NM_001277269.1:c.520G= NP_001264198.1:p.Gly174=
NM_001292063.1:c.484G= NP_001278992.1:p.Gly162=
NM_001277269.2:c.520G= NP_001264198.1:p.Gly174=
NM_001292063.2:c.484G= MANE Select NP_001278992.1:p.Gly162=