Canonical Allele Identifier: CA2574771172

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17635245_17635246del , CM000673.2:g.17635245_17635246del	GRCh38
NC_000011.9:g.17656792_17656793del , CM000673.1:g.17656792_17656793del	GRCh37
NC_000011.8:g.17613368_17613369del	NCBI36
NG_033191.1:g.92873_92874del
NG_033191.2:g.92873_92874del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7729+58_7729+59del	ENSP00000382323.2:n.7729+58_7729+59del
ENST00000399397.6:c.7693+58_7693+59del MANE Select	ENSP00000382329.2:n.7693+58_7693+59del
ENST00000342528.2:c.4322-365_4322-364del	ENSP00000341666.2:n.4322-365_4322-364del
ENST00000399391.6:c.7729+58_7729+59del	ENSP00000382323.2:n.7729+58_7729+59del
ENST00000399397.5:c.7693+58_7693+59del	ENSP00000382329.2:n.7693+58_7693+59del
NM_001277269.1:c.7729+58_7729+59del	NP_001264198.1:n.7729+58_7729+59del
NM_001292063.1:c.7693+58_7693+59del	NP_001278992.1:n.7693+58_7693+59del
NM_001277269.2:c.7729+58_7729+59del	NP_001264198.1:n.7729+58_7729+59del
NM_001292063.2:c.7693+58_7693+59del MANE Select	NP_001278992.1:n.7693+58_7693+59del