Canonical Allele Identifier: CA674246190

Gene: OTOG

Linked Data

• dbSNP Id: rs1415039865
• gnomAD v3: 11-17553052-AG-A
• gnomAD v4: 11-17553052-AG-A
• MyVariant Identifiers: chr11:g.17574600del (hg19) ; chr11:g.17553053del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553055del , CM000673.2:g.17553055del	GRCh38
NC_000011.9:g.17574602del , CM000673.1:g.17574602del	GRCh37
NC_000011.8:g.17531178del	NCBI36
NG_033191.1:g.10683del
NG_033191.2:g.10683del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.329-64del	ENSP00000382323.2:n.329-64del
ENST00000399397.6:c.293-64del MANE Select	ENSP00000382329.2:n.293-64del
ENST00000399391.6:c.329-64del	ENSP00000382323.2:n.329-64del
ENST00000399397.5:c.293-64del	ENSP00000382329.2:n.293-64del
ENST00000428619.1:c.110-64del	ENSP00000399057.2:n.110-64del
ENST00000498332.5:n.199-64del
NM_001277269.1:c.329-64del	NP_001264198.1:n.329-64del
NM_001292063.1:c.293-64del	NP_001278992.1:n.293-64del
NM_001277269.2:c.329-64del	NP_001264198.1:n.329-64del
NM_001292063.2:c.293-64del MANE Select	NP_001278992.1:n.293-64del