Canonical Allele Identifier: CA1955197679

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553256_17553257delinsAG , CM000673.2:g.17553256_17553257delinsAG	GRCh38
NC_000011.9:g.17574803_17574804delinsAG , CM000673.1:g.17574803_17574804delinsAG	GRCh37
NC_000011.8:g.17531379_17531380delinsAG	NCBI36
NG_033191.1:g.10884_10885delinsAG
NG_033191.2:g.10884_10885delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.421+45_421+46delinsAG	ENSP00000382323.2:n.421+45_421+46delinsAG
ENST00000399397.6:c.385+45_385+46delinsAG MANE Select	ENSP00000382329.2:n.385+45_385+46delinsAG
ENST00000399391.6:c.421+45_421+46delinsAG	ENSP00000382323.2:n.421+45_421+46delinsAG
ENST00000399397.5:c.385+45_385+46delinsAG	ENSP00000382329.2:n.385+45_385+46delinsAG
ENST00000428619.1:c.202+45_202+46delinsAG	ENSP00000399057.2:n.202+45_202+46delinsAG
ENST00000498332.5:n.291+45_291+46delinsAG
NM_001277269.1:c.421+45_421+46delinsAG	NP_001264198.1:n.421+45_421+46delinsAG
NM_001292063.1:c.385+45_385+46delinsAG	NP_001278992.1:n.385+45_385+46delinsAG
NM_001277269.2:c.421+45_421+46delinsAG	NP_001264198.1:n.421+45_421+46delinsAG
NM_001292063.2:c.385+45_385+46delinsAG MANE Select	NP_001278992.1:n.385+45_385+46delinsAG