Canonical Allele Identifier: CA1955197757
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553406_17553407delinsTG , CM000673.2:g.17553406_17553407delinsTG GRCh38
NC_000011.9:g.17574953_17574954delinsTG , CM000673.1:g.17574953_17574954delinsTG GRCh37
NC_000011.8:g.17531529_17531530delinsTG NCBI36
NG_033191.1:g.11034_11035delinsTG
NG_033191.2:g.11034_11035delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.463_464delinsTG ENSP00000382323.2:p.Trp155=
ENST00000399397.6:c.427_428delinsTG MANE Select ENSP00000382329.2:p.Trp143=
ENST00000399391.6:c.463_464delinsTG ENSP00000382323.2:p.Trp155=
ENST00000399397.5:c.427_428delinsTG ENSP00000382329.2:p.Trp143=
ENST00000428619.1:c.244_245delinsTG ENSP00000399057.2:p.Trp82=
ENST00000498332.5:n.333_334delinsTG
NM_001277269.1:c.463_464delinsTG NP_001264198.1:p.Trp155=
NM_001292063.1:c.427_428delinsTG NP_001278992.1:p.Trp143=
NM_001277269.2:c.463_464delinsTG NP_001264198.1:p.Trp155=
NM_001292063.2:c.427_428delinsTG MANE Select NP_001278992.1:p.Trp143=