Canonical Allele Identifier: CA1955197802
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553495C= , CM000673.2:g.17553495C= GRCh38
NC_000011.9:g.17575042C= , CM000673.1:g.17575042C= GRCh37
NC_000011.8:g.17531618C= NCBI36
NG_033191.1:g.11123C=
NG_033191.2:g.11123C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.552C= ENSP00000382323.2:p.Pro184=
ENST00000399397.6:c.516C= MANE Select ENSP00000382329.2:p.Pro172=
ENST00000399391.6:c.552C= ENSP00000382323.2:p.Pro184=
ENST00000399397.5:c.516C= ENSP00000382329.2:p.Pro172=
ENST00000498332.5:n.422C=
NM_001277269.1:c.552C= NP_001264198.1:p.Pro184=
NM_001292063.1:c.516C= NP_001278992.1:p.Pro172=
NM_001277269.2:c.552C= NP_001264198.1:p.Pro184=
NM_001292063.2:c.516C= MANE Select NP_001278992.1:p.Pro172=