Canonical Allele Identifier: CA2612679626

Gene: OTOG

Linked Data

• gnomAD v4: 11-17553440-TCTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553448_17553450del , CM000673.2:g.17553448_17553450del	GRCh38
NC_000011.9:g.17574995_17574997del , CM000673.1:g.17574995_17574997del	GRCh37
NC_000011.8:g.17531571_17531573del	NCBI36
NG_033191.1:g.11076_11078del
NG_033191.2:g.11076_11078del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.505_507del	ENSP00000382323.2:p.Tyr169del
ENST00000399397.6:c.469_471del MANE Select	ENSP00000382329.2:p.Tyr157del
ENST00000399391.6:c.505_507del	ENSP00000382323.2:p.Tyr169del
ENST00000399397.5:c.469_471del	ENSP00000382329.2:p.Tyr157del
ENST00000498332.5:n.375_377del
NM_001277269.1:c.505_507del	NP_001264198.1:p.Tyr169del
NM_001292063.1:c.469_471del	NP_001278992.1:p.Tyr157del
NM_001277269.2:c.505_507del	NP_001264198.1:p.Tyr169del
NM_001292063.2:c.469_471del MANE Select	NP_001278992.1:p.Tyr157del