Canonical Allele Identifier: CA379813041
Gene: OTOG HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.17656693C>A (hg19) chr11:g.17635146C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17635146C>A , CM000673.2:g.17635146C>A GRCh38
NC_000011.9:g.17656693C>A , CM000673.1:g.17656693C>A GRCh37
NC_000011.8:g.17613269C>A NCBI36
NG_033191.1:g.92774C>A
NG_033191.2:g.92774C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.7688C>A ENSP00000382323.2:p.Thr2563Lys
ENST00000399397.6:c.7652C>A MANE Select ENSP00000382329.2:p.Thr2551Lys
ENST00000342528.2:c.4322-464C>A ENSP00000341666.2:n.4322-464C>A
ENST00000399391.6:c.7688C>A ENSP00000382323.2:p.Thr2563Lys
ENST00000399397.5:c.7652C>A ENSP00000382329.2:p.Thr2551Lys
NM_001277269.1:c.7688C>A NP_001264198.1:p.Thr2563Lys
NM_001292063.1:c.7652C>A NP_001278992.1:p.Thr2551Lys
NM_001277269.2:c.7688C>A NP_001264198.1:p.Thr2563Lys
NM_001292063.2:c.7652C>A MANE Select NP_001278992.1:p.Thr2551Lys
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