Canonical Allele Identifier: CA935545076

Gene: OTOG

Linked Data

• gnomAD v3: 11-17634959-C-CGG
• gnomAD v4: 11-17634959-C-CGG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17634962_17634963dup , CM000673.2:g.17634962_17634963dup	GRCh38
NC_000011.9:g.17656509_17656510dup , CM000673.1:g.17656509_17656510dup	GRCh37
NC_000011.8:g.17613085_17613086dup	NCBI36
NG_033191.1:g.92590_92591dup
NG_033191.2:g.92590_92591dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7621+14_7621+15dup	ENSP00000382323.2:n.7621+14_7621+15dup
ENST00000399397.6:c.7585+14_7585+15dup MANE Select	ENSP00000382329.2:n.7585+14_7585+15dup
ENST00000342528.2:c.4322-648_4322-647dup	ENSP00000341666.2:n.4322-648_4322-647dup
ENST00000399391.6:c.7621+14_7621+15dup	ENSP00000382323.2:n.7621+14_7621+15dup
ENST00000399397.5:c.7585+14_7585+15dup	ENSP00000382329.2:n.7585+14_7585+15dup
NM_001277269.1:c.7621+14_7621+15dup	NP_001264198.1:n.7621+14_7621+15dup
NM_001292063.1:c.7585+14_7585+15dup	NP_001278992.1:n.7585+14_7585+15dup
NM_001277269.2:c.7621+14_7621+15dup	NP_001264198.1:n.7621+14_7621+15dup
NM_001292063.2:c.7585+14_7585+15dup MANE Select	NP_001278992.1:n.7585+14_7585+15dup