Canonical Allele Identifier: CA1955197742
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553378C= , CM000673.2:g.17553378C= GRCh38
NC_000011.9:g.17574925C= , CM000673.1:g.17574925C= GRCh37
NC_000011.8:g.17531501C= NCBI36
NG_033191.1:g.11006C=
NG_033191.2:g.11006C=

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.435C= ENSP00000382323.2:p.Gly145=
ENST00000399397.6:c.399C= MANE Select ENSP00000382329.2:p.Gly133=
ENST00000399391.6:c.435C= ENSP00000382323.2:p.Gly145=
ENST00000399397.5:c.399C= ENSP00000382329.2:p.Gly133=
ENST00000428619.1:c.216C= ENSP00000399057.2:p.Gly72=
ENST00000498332.5:n.305C=
NM_001277269.1:c.435C= NP_001264198.1:p.Gly145=
NM_001292063.1:c.399C= NP_001278992.1:p.Gly133=
NM_001277269.2:c.435C= NP_001264198.1:p.Gly145=
NM_001292063.2:c.399C= MANE Select NP_001278992.1:p.Gly133=