Canonical Allele Identifier: CA1955197851
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553599_17553603delinsATAGT , CM000673.2:g.17553599_17553603delinsATAGT GRCh38
NC_000011.9:g.17575146_17575150delinsATAGT , CM000673.1:g.17575146_17575150delinsATAGT GRCh37
NC_000011.8:g.17531722_17531726delinsATAGT NCBI36
NG_033191.1:g.11227_11231delinsATAGT
NG_033191.2:g.11227_11231delinsATAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.576+80_576+84delinsATAGT ENSP00000382323.2:n.576+80_576+84delinsATAGT
ENST00000399397.6:c.540+80_540+84delinsATAGT MANE Select ENSP00000382329.2:n.540+80_540+84delinsATAGT
ENST00000399391.6:c.576+80_576+84delinsATAGT ENSP00000382323.2:n.576+80_576+84delinsATAGT
ENST00000399397.5:c.540+80_540+84delinsATAGT ENSP00000382329.2:n.540+80_540+84delinsATAGT
ENST00000498332.5:n.446+80_446+84delinsATAGT
NM_001277269.1:c.576+80_576+84delinsATAGT NP_001264198.1:n.576+80_576+84delinsATAGT
NM_001292063.1:c.540+80_540+84delinsATAGT NP_001278992.1:n.540+80_540+84delinsATAGT
NM_001277269.2:c.576+80_576+84delinsATAGT NP_001264198.1:n.576+80_576+84delinsATAGT
NM_001292063.2:c.540+80_540+84delinsATAGT MANE Select NP_001278992.1:n.540+80_540+84delinsATAGT