Canonical Allele Identifier: CA2612690044

Gene: OTOG

Linked Data

• gnomAD v4: 11-17635025-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17635026del , CM000673.2:g.17635026del	GRCh38
NC_000011.9:g.17656573del , CM000673.1:g.17656573del	GRCh37
NC_000011.8:g.17613149del	NCBI36
NG_033191.1:g.92654del
NG_033191.2:g.92654del

Transcript Alleles

HGVS	Amino-acid change
ENST00000399391.7:c.7622-54del	ENSP00000382323.2:n.7622-54del
ENST00000399397.6:c.7586-54del MANE Select	ENSP00000382329.2:n.7586-54del
ENST00000342528.2:c.4322-584del	ENSP00000341666.2:n.4322-584del
ENST00000399391.6:c.7622-54del	ENSP00000382323.2:n.7622-54del
ENST00000399397.5:c.7586-54del	ENSP00000382329.2:n.7586-54del
NM_001277269.1:c.7622-54del	NP_001264198.1:n.7622-54del
NM_001292063.1:c.7586-54del	NP_001278992.1:n.7586-54del
NM_001277269.2:c.7622-54del	NP_001264198.1:n.7622-54del
NM_001292063.2:c.7586-54del MANE Select	NP_001278992.1:n.7586-54del