Canonical Allele Identifier: CA1955197771
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553434A= , CM000673.2:g.17553434A= GRCh38
NC_000011.9:g.17574981A= , CM000673.1:g.17574981A= GRCh37
NC_000011.8:g.17531557A= NCBI36
NG_033191.1:g.11062A=
NG_033191.2:g.11062A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.491A= ENSP00000382323.2:p.Asp164=
ENST00000399397.6:c.455A= MANE Select ENSP00000382329.2:p.Asp152=
ENST00000399391.6:c.491A= ENSP00000382323.2:p.Asp164=
ENST00000399397.5:c.455A= ENSP00000382329.2:p.Asp152=
ENST00000428619.1:c.272A= ENSP00000399057.2:p.Asp91=
ENST00000498332.5:n.361A=
NM_001277269.1:c.491A= NP_001264198.1:p.Asp164=
NM_001292063.1:c.455A= NP_001278992.1:p.Asp152=
NM_001277269.2:c.491A= NP_001264198.1:p.Asp164=
NM_001292063.2:c.455A= MANE Select NP_001278992.1:p.Asp152=