Canonical Allele Identifier: CA2612679106
Gene: OTOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553023_17553024del , CM000673.2:g.17553023_17553024del GRCh38
NC_000011.9:g.17574570_17574571del , CM000673.1:g.17574570_17574571del GRCh37
NC_000011.8:g.17531146_17531147del NCBI36
NG_033191.1:g.10651_10652del
NG_033191.2:g.10651_10652del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.329-96_329-95del ENSP00000382323.2:n.329-96_329-95del
ENST00000399397.6:c.293-96_293-95del MANE Select ENSP00000382329.2:n.293-96_293-95del
ENST00000399391.6:c.329-96_329-95del ENSP00000382323.2:n.329-96_329-95del
ENST00000399397.5:c.293-96_293-95del ENSP00000382329.2:n.293-96_293-95del
ENST00000428619.1:c.110-96_110-95del ENSP00000399057.2:n.110-96_110-95del
ENST00000498332.5:n.199-96_199-95del
NM_001277269.1:c.329-96_329-95del NP_001264198.1:n.329-96_329-95del
NM_001292063.1:c.293-96_293-95del NP_001278992.1:n.293-96_293-95del
NM_001277269.2:c.329-96_329-95del NP_001264198.1:n.329-96_329-95del
NM_001292063.2:c.293-96_293-95del MANE Select NP_001278992.1:n.293-96_293-95del