Canonical Allele Identifier: CA1955197773
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553439C= , CM000673.2:g.17553439C= GRCh38
NC_000011.9:g.17574986C= , CM000673.1:g.17574986C= GRCh37
NC_000011.8:g.17531562C= NCBI36
NG_033191.1:g.11067C=
NG_033191.2:g.11067C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.496C= ENSP00000382323.2:p.Leu166=
ENST00000399397.6:c.460C= MANE Select ENSP00000382329.2:p.Leu154=
ENST00000399391.6:c.496C= ENSP00000382323.2:p.Leu166=
ENST00000399397.5:c.460C= ENSP00000382329.2:p.Leu154=
ENST00000428619.1:c.277C= ENSP00000399057.2:p.Leu93=
ENST00000498332.5:n.366C=
NM_001277269.1:c.496C= NP_001264198.1:p.Leu166=
NM_001292063.1:c.460C= NP_001278992.1:p.Leu154=
NM_001277269.2:c.496C= NP_001264198.1:p.Leu166=
NM_001292063.2:c.460C= MANE Select NP_001278992.1:p.Leu154=