Canonical Allele Identifier: CA1955197683
Gene: OTOG HGNC NCBI

Linked Data

dbSNP Id: rs1851983583
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553264C>A , CM000673.2:g.17553264C>A GRCh38
NC_000011.9:g.17574811C>A , CM000673.1:g.17574811C>A GRCh37
NC_000011.8:g.17531387C>A NCBI36
NG_033191.1:g.10892C>A
NG_033191.2:g.10892C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.421+53C>A ENSP00000382323.2:n.421+53C>A
ENST00000399397.6:c.385+53C>A MANE Select ENSP00000382329.2:n.385+53C>A
ENST00000399391.6:c.421+53C>A ENSP00000382323.2:n.421+53C>A
ENST00000399397.5:c.385+53C>A ENSP00000382329.2:n.385+53C>A
ENST00000428619.1:c.202+53C>A ENSP00000399057.2:n.202+53C>A
ENST00000498332.5:n.291+53C>A
NM_001277269.1:c.421+53C>A NP_001264198.1:n.421+53C>A
NM_001292063.1:c.385+53C>A NP_001278992.1:n.385+53C>A
NM_001277269.2:c.421+53C>A NP_001264198.1:n.421+53C>A
NM_001292063.2:c.385+53C>A MANE Select NP_001278992.1:n.385+53C>A
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