Canonical Allele Identifier: CA2830555110
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553669_17553670del , CM000673.2:g.17553669_17553670del GRCh38
NC_000011.9:g.17575216_17575217del , CM000673.1:g.17575216_17575217del GRCh37
NC_000011.8:g.17531792_17531793del NCBI36
NG_033191.1:g.11297_11298del
NG_033191.2:g.11297_11298del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.576+150_576+151del ENSP00000382323.2:n.576+150_576+151del
ENST00000399397.6:c.540+150_540+151del MANE Select ENSP00000382329.2:n.540+150_540+151del
ENST00000399391.6:c.576+150_576+151del ENSP00000382323.2:n.576+150_576+151del
ENST00000399397.5:c.540+150_540+151del ENSP00000382329.2:n.540+150_540+151del
ENST00000498332.5:n.446+150_446+151del
NM_001277269.1:c.576+150_576+151del NP_001264198.1:n.576+150_576+151del
NM_001292063.1:c.540+150_540+151del NP_001278992.1:n.540+150_540+151del
NM_001277269.2:c.576+150_576+151del NP_001264198.1:n.576+150_576+151del
NM_001292063.2:c.540+150_540+151del MANE Select NP_001278992.1:n.540+150_540+151del