Canonical Allele Identifier: CA1955197596
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553123G= , CM000673.2:g.17553123G= GRCh38
NC_000011.9:g.17574670G= , CM000673.1:g.17574670G= GRCh37
NC_000011.8:g.17531246G= NCBI36
NG_033191.1:g.10751G=
NG_033191.2:g.10751G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.333G= ENSP00000382323.2:p.Leu111=
ENST00000399397.6:c.297G= MANE Select ENSP00000382329.2:p.Leu99=
ENST00000399391.6:c.333G= ENSP00000382323.2:p.Leu111=
ENST00000399397.5:c.297G= ENSP00000382329.2:p.Leu99=
ENST00000428619.1:c.114G= ENSP00000399057.2:p.Leu38=
ENST00000498332.5:n.203G=
NM_001277269.1:c.333G= NP_001264198.1:p.Leu111=
NM_001292063.1:c.297G= NP_001278992.1:p.Leu99=
NM_001277269.2:c.333G= NP_001264198.1:p.Leu111=
NM_001292063.2:c.297G= MANE Select NP_001278992.1:p.Leu99=