Canonical Allele Identifier: CA379803885

Gene: OTOG

Linked Data

• gnomAD v4: 11-17612297-G-T
• MyVariant Identifiers: chr11:g.17633844G>T (hg19) ; chr11:g.17612297G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612297G>T , CM000673.2:g.17612297G>T	GRCh38
NC_000011.9:g.17633844G>T , CM000673.1:g.17633844G>T	GRCh37
NC_000011.8:g.17590420G>T	NCBI36
NG_033191.1:g.69925G>T
NG_033191.2:g.69925G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6295G>T	ENSP00000382323.2:p.Gly2099Trp
ENST00000399397.6:c.6259G>T MANE Select	ENSP00000382329.2:p.Gly2087Trp
ENST00000342528.2:c.3313G>T	ENSP00000341666.2:p.Gly1105Trp
ENST00000399391.6:c.6295G>T	ENSP00000382323.2:p.Gly2099Trp
ENST00000399397.5:c.6259G>T	ENSP00000382329.2:p.Gly2087Trp
NM_001277269.1:c.6295G>T	NP_001264198.1:p.Gly2099Trp
NM_001292063.1:c.6259G>T	NP_001278992.1:p.Gly2087Trp
NM_001277269.2:c.6295G>T	NP_001264198.1:p.Gly2099Trp
NM_001292063.2:c.6259G>T MANE Select	NP_001278992.1:p.Gly2087Trp