Canonical Allele Identifier: CA918828350

Gene: OTOG

Linked Data

• dbSNP Id: rs1565128366
• gnomAD v4: 11-17635279-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17635284del , CM000673.2:g.17635284del	GRCh38
NC_000011.9:g.17656831del , CM000673.1:g.17656831del	GRCh37
NC_000011.8:g.17613407del	NCBI36
NG_033191.1:g.92912del
NG_033191.2:g.92912del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7729+97del	ENSP00000382323.2:n.7729+97del
ENST00000399397.6:c.7693+97del MANE Select	ENSP00000382329.2:n.7693+97del
ENST00000342528.2:c.4322-326del	ENSP00000341666.2:n.4322-326del
ENST00000399391.6:c.7729+97del	ENSP00000382323.2:n.7729+97del
ENST00000399397.5:c.7693+97del	ENSP00000382329.2:n.7693+97del
NM_001277269.1:c.7729+97del	NP_001264198.1:n.7729+97del
NM_001292063.1:c.7693+97del	NP_001278992.1:n.7693+97del
NM_001277269.2:c.7729+97del	NP_001264198.1:n.7729+97del
NM_001292063.2:c.7693+97del MANE Select	NP_001278992.1:n.7693+97del