Canonical Allele Identifier: CA597675726

Gene: OTOG

Linked Data

• dbSNP Id: rs1175710943
• gnomAD v2: 11-17656511-T-G
• gnomAD v3: 11-17634964-T-G
• gnomAD v4: 11-17634964-T-G
• MyVariant Identifiers: chr11:g.17656511T>G (hg19) ; chr11:g.17634964T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17634964T>G , CM000673.2:g.17634964T>G	GRCh38
NC_000011.9:g.17656511T>G , CM000673.1:g.17656511T>G	GRCh37
NC_000011.8:g.17613087T>G	NCBI36
NG_033191.1:g.92592T>G
NG_033191.2:g.92592T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7621+16T>G	ENSP00000382323.2:n.7621+16T>G
ENST00000399397.6:c.7585+16T>G MANE Select	ENSP00000382329.2:n.7585+16T>G
ENST00000342528.2:c.4322-646T>G	ENSP00000341666.2:n.4322-646T>G
ENST00000399391.6:c.7621+16T>G	ENSP00000382323.2:n.7621+16T>G
ENST00000399397.5:c.7585+16T>G	ENSP00000382329.2:n.7585+16T>G
NM_001277269.1:c.7621+16T>G	NP_001264198.1:n.7621+16T>G
NM_001292063.1:c.7585+16T>G	NP_001278992.1:n.7585+16T>G
NM_001277269.2:c.7621+16T>G	NP_001264198.1:n.7621+16T>G
NM_001292063.2:c.7585+16T>G MANE Select	NP_001278992.1:n.7585+16T>G