Canonical Allele Identifier: CA1955197652

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553227_17553228delinsAC , CM000673.2:g.17553227_17553228delinsAC	GRCh38
NC_000011.9:g.17574774_17574775delinsAC , CM000673.1:g.17574774_17574775delinsAC	GRCh37
NC_000011.8:g.17531350_17531351delinsAC	NCBI36
NG_033191.1:g.10855_10856delinsAC
NG_033191.2:g.10855_10856delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.421+16_421+17delinsAC	ENSP00000382323.2:n.421+16_421+17delinsAC
ENST00000399397.6:c.385+16_385+17delinsAC MANE Select	ENSP00000382329.2:n.385+16_385+17delinsAC
ENST00000399391.6:c.421+16_421+17delinsAC	ENSP00000382323.2:n.421+16_421+17delinsAC
ENST00000399397.5:c.385+16_385+17delinsAC	ENSP00000382329.2:n.385+16_385+17delinsAC
ENST00000428619.1:c.202+16_202+17delinsAC	ENSP00000399057.2:n.202+16_202+17delinsAC
ENST00000498332.5:n.291+16_291+17delinsAC
NM_001277269.1:c.421+16_421+17delinsAC	NP_001264198.1:n.421+16_421+17delinsAC
NM_001292063.1:c.385+16_385+17delinsAC	NP_001278992.1:n.385+16_385+17delinsAC
NM_001277269.2:c.421+16_421+17delinsAC	NP_001264198.1:n.421+16_421+17delinsAC
NM_001292063.2:c.385+16_385+17delinsAC MANE Select	NP_001278992.1:n.385+16_385+17delinsAC