Canonical Allele Identifier: CA1955237062
Gene: OTOG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17635351A= , CM000673.2:g.17635351A= GRCh38
NC_000011.9:g.17656898A= , CM000673.1:g.17656898A= GRCh37
NC_000011.8:g.17613474A= NCBI36
NG_033191.1:g.92979A=
NG_033191.2:g.92979A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.7729+164A= ENSP00000382323.2:n.7729+164A=
ENST00000399397.6:c.7693+164A= MANE Select ENSP00000382329.2:n.7693+164A=
ENST00000342528.2:c.4322-259A= ENSP00000341666.2:n.4322-259A=
ENST00000399391.6:c.7729+164A= ENSP00000382323.2:n.7729+164A=
ENST00000399397.5:c.7693+164A= ENSP00000382329.2:n.7693+164A=
NM_001277269.1:c.7729+164A= NP_001264198.1:n.7729+164A=
NM_001292063.1:c.7693+164A= NP_001278992.1:n.7693+164A=
NM_001277269.2:c.7729+164A= NP_001264198.1:n.7729+164A=
NM_001292063.2:c.7693+164A= MANE Select NP_001278992.1:n.7693+164A=
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