Canonical Allele Identifier: CA1955237023

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17635279_17635280delinsTG , CM000673.2:g.17635279_17635280delinsTG	GRCh38
NC_000011.9:g.17656826_17656827delinsTG , CM000673.1:g.17656826_17656827delinsTG	GRCh37
NC_000011.8:g.17613402_17613403delinsTG	NCBI36
NG_033191.1:g.92907_92908delinsTG
NG_033191.2:g.92907_92908delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7729+92_7729+93delinsTG	ENSP00000382323.2:n.7729+92_7729+93delinsTG
ENST00000399397.6:c.7693+92_7693+93delinsTG MANE Select	ENSP00000382329.2:n.7693+92_7693+93delinsTG
ENST00000342528.2:c.4322-331_4322-330delinsTG	ENSP00000341666.2:n.4322-331_4322-330delinsTG
ENST00000399391.6:c.7729+92_7729+93delinsTG	ENSP00000382323.2:n.7729+92_7729+93delinsTG
ENST00000399397.5:c.7693+92_7693+93delinsTG	ENSP00000382329.2:n.7693+92_7693+93delinsTG
NM_001277269.1:c.7729+92_7729+93delinsTG	NP_001264198.1:n.7729+92_7729+93delinsTG
NM_001292063.1:c.7693+92_7693+93delinsTG	NP_001278992.1:n.7693+92_7693+93delinsTG
NM_001277269.2:c.7729+92_7729+93delinsTG	NP_001264198.1:n.7729+92_7729+93delinsTG
NM_001292063.2:c.7693+92_7693+93delinsTG MANE Select	NP_001278992.1:n.7693+92_7693+93delinsTG