Canonical Allele Identifier: CA2612679155

Gene: OTOG

Linked Data

• gnomAD v4: 11-17553033-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553033_17553034insC , CM000673.2:g.17553033_17553034insC	GRCh38
NC_000011.9:g.17574580_17574581insC , CM000673.1:g.17574580_17574581insC	GRCh37
NC_000011.8:g.17531156_17531157insC	NCBI36
NG_033191.1:g.10661_10662insC
NG_033191.2:g.10661_10662insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.329-86_329-85insC	ENSP00000382323.2:n.329-86_329-85insC
ENST00000399397.6:c.293-86_293-85insC MANE Select	ENSP00000382329.2:n.293-86_293-85insC
ENST00000399391.6:c.329-86_329-85insC	ENSP00000382323.2:n.329-86_329-85insC
ENST00000399397.5:c.293-86_293-85insC	ENSP00000382329.2:n.293-86_293-85insC
ENST00000428619.1:c.110-86_110-85insC	ENSP00000399057.2:n.110-86_110-85insC
ENST00000498332.5:n.199-86_199-85insC
NM_001277269.1:c.329-86_329-85insC	NP_001264198.1:n.329-86_329-85insC
NM_001292063.1:c.293-86_293-85insC	NP_001278992.1:n.293-86_293-85insC
NM_001277269.2:c.329-86_329-85insC	NP_001264198.1:n.329-86_329-85insC
NM_001292063.2:c.293-86_293-85insC MANE Select	NP_001278992.1:n.293-86_293-85insC