Canonical Allele Identifier: CA1955237027
Gene: OTOG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17635285T= , CM000673.2:g.17635285T= GRCh38
NC_000011.9:g.17656832T= , CM000673.1:g.17656832T= GRCh37
NC_000011.8:g.17613408T= NCBI36
NG_033191.1:g.92913T=
NG_033191.2:g.92913T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.7729+98T= ENSP00000382323.2:n.7729+98T=
ENST00000399397.6:c.7693+98T= MANE Select ENSP00000382329.2:n.7693+98T=
ENST00000342528.2:c.4322-325T= ENSP00000341666.2:n.4322-325T=
ENST00000399391.6:c.7729+98T= ENSP00000382323.2:n.7729+98T=
ENST00000399397.5:c.7693+98T= ENSP00000382329.2:n.7693+98T=
NM_001277269.1:c.7729+98T= NP_001264198.1:n.7729+98T=
NM_001292063.1:c.7693+98T= NP_001278992.1:n.7693+98T=
NM_001277269.2:c.7729+98T= NP_001264198.1:n.7729+98T=
NM_001292063.2:c.7693+98T= MANE Select NP_001278992.1:n.7693+98T=
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