Canonical Allele Identifier: CA379812798
Gene: OTOG HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.17656480C>A (hg19) chr11:g.17634933C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17634933C>A , CM000673.2:g.17634933C>A GRCh38
NC_000011.9:g.17656480C>A , CM000673.1:g.17656480C>A GRCh37
NC_000011.8:g.17613056C>A NCBI36
NG_033191.1:g.92561C>A
NG_033191.2:g.92561C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.7606C>A ENSP00000382323.2:p.Pro2536Thr
ENST00000399397.6:c.7570C>A MANE Select ENSP00000382329.2:p.Pro2524Thr
ENST00000342528.2:c.4322-677C>A ENSP00000341666.2:n.4322-677C>A
ENST00000399391.6:c.7606C>A ENSP00000382323.2:p.Pro2536Thr
ENST00000399397.5:c.7570C>A ENSP00000382329.2:p.Pro2524Thr
NM_001277269.1:c.7606C>A NP_001264198.1:p.Pro2536Thr
NM_001292063.1:c.7570C>A NP_001278992.1:p.Pro2524Thr
NM_001277269.2:c.7606C>A NP_001264198.1:p.Pro2536Thr
NM_001292063.2:c.7570C>A MANE Select NP_001278992.1:p.Pro2524Thr
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