Canonical Allele Identifier: CA1955197879
Gene: OTOG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553638C= , CM000673.2:g.17553638C= GRCh38
NC_000011.9:g.17575185C= , CM000673.1:g.17575185C= GRCh37
NC_000011.8:g.17531761C= NCBI36
NG_033191.1:g.11266C=
NG_033191.2:g.11266C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.576+119C= ENSP00000382323.2:n.576+119C=
ENST00000399397.6:c.540+119C= MANE Select ENSP00000382329.2:n.540+119C=
ENST00000399391.6:c.576+119C= ENSP00000382323.2:n.576+119C=
ENST00000399397.5:c.540+119C= ENSP00000382329.2:n.540+119C=
ENST00000498332.5:n.446+119C=
NM_001277269.1:c.576+119C= NP_001264198.1:n.576+119C=
NM_001292063.1:c.540+119C= NP_001278992.1:n.540+119C=
NM_001277269.2:c.576+119C= NP_001264198.1:n.576+119C=
NM_001292063.2:c.540+119C= MANE Select NP_001278992.1:n.540+119C=
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