Canonical Allele Identifier: CA2612679205

Gene: OTOG

Linked Data

• gnomAD v4: 11-17553048-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553052_17553053del , CM000673.2:g.17553052_17553053del	GRCh38
NC_000011.9:g.17574599_17574600del , CM000673.1:g.17574599_17574600del	GRCh37
NC_000011.8:g.17531175_17531176del	NCBI36
NG_033191.1:g.10680_10681del
NG_033191.2:g.10680_10681del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.329-67_329-66del	ENSP00000382323.2:n.329-67_329-66del
ENST00000399397.6:c.293-67_293-66del MANE Select	ENSP00000382329.2:n.293-67_293-66del
ENST00000399391.6:c.329-67_329-66del	ENSP00000382323.2:n.329-67_329-66del
ENST00000399397.5:c.293-67_293-66del	ENSP00000382329.2:n.293-67_293-66del
ENST00000428619.1:c.110-67_110-66del	ENSP00000399057.2:n.110-67_110-66del
ENST00000498332.5:n.199-67_199-66del
NM_001277269.1:c.329-67_329-66del	NP_001264198.1:n.329-67_329-66del
NM_001292063.1:c.293-67_293-66del	NP_001278992.1:n.293-67_293-66del
NM_001277269.2:c.329-67_329-66del	NP_001264198.1:n.329-67_329-66del
NM_001292063.2:c.293-67_293-66del MANE Select	NP_001278992.1:n.293-67_293-66del