Canonical Allele Identifier: CA1955197759
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553411G= , CM000673.2:g.17553411G= GRCh38
NC_000011.9:g.17574958G= , CM000673.1:g.17574958G= GRCh37
NC_000011.8:g.17531534G= NCBI36
NG_033191.1:g.11039G=
NG_033191.2:g.11039G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.468G= ENSP00000382323.2:p.Gly156=
ENST00000399397.6:c.432G= MANE Select ENSP00000382329.2:p.Gly144=
ENST00000399391.6:c.468G= ENSP00000382323.2:p.Gly156=
ENST00000399397.5:c.432G= ENSP00000382329.2:p.Gly144=
ENST00000428619.1:c.249G= ENSP00000399057.2:p.Gly83=
ENST00000498332.5:n.338G=
NM_001277269.1:c.468G= NP_001264198.1:p.Gly156=
NM_001292063.1:c.432G= NP_001278992.1:p.Gly144=
NM_001277269.2:c.468G= NP_001264198.1:p.Gly156=
NM_001292063.2:c.432G= MANE Select NP_001278992.1:p.Gly144=