Canonical Allele Identifier: CA1955242343
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17645852C= , CM000673.2:g.17645852C= GRCh38
NC_000011.9:g.17667399C= , CM000673.1:g.17667399C= GRCh37
NC_000011.8:g.17623975C= NCBI36
NG_033191.1:g.103480C=
NG_033191.2:g.103480C=

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.8686C= ENSP00000382323.2:p.Arg2896=
ENST00000399397.6:c.8650C= MANE Select ENSP00000382329.2:p.Arg2884=
ENST00000399391.6:c.8686C= ENSP00000382323.2:p.Arg2896=
ENST00000399397.5:c.8650C= ENSP00000382329.2:p.Arg2884=
NM_001277269.1:c.8686C= NP_001264198.1:p.Arg2896=
NM_001292063.1:c.8650C= NP_001278992.1:p.Arg2884=
NM_001277269.2:c.8686C= NP_001264198.1:p.Arg2896=
NM_001292063.2:c.8650C= MANE Select NP_001278992.1:p.Arg2884=