Canonical Allele Identifier: CA1955197796
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553484C= , CM000673.2:g.17553484C= GRCh38
NC_000011.9:g.17575031C= , CM000673.1:g.17575031C= GRCh37
NC_000011.8:g.17531607C= NCBI36
NG_033191.1:g.11112C=
NG_033191.2:g.11112C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.541C= ENSP00000382323.2:p.Arg181=
ENST00000399397.6:c.505C= MANE Select ENSP00000382329.2:p.Arg169=
ENST00000399391.6:c.541C= ENSP00000382323.2:p.Arg181=
ENST00000399397.5:c.505C= ENSP00000382329.2:p.Arg169=
ENST00000498332.5:n.411C=
NM_001277269.1:c.541C= NP_001264198.1:p.Arg181=
NM_001292063.1:c.505C= NP_001278992.1:p.Arg169=
NM_001277269.2:c.541C= NP_001264198.1:p.Arg181=
NM_001292063.2:c.505C= MANE Select NP_001278992.1:p.Arg169=