Canonical Allele Identifier: CA1955232888
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17612329_17612331delinsCTG , CM000673.2:g.17612329_17612331delinsCTG GRCh38
NC_000011.9:g.17633876_17633878delinsCTG , CM000673.1:g.17633876_17633878delinsCTG GRCh37
NC_000011.8:g.17590452_17590454delinsCTG NCBI36
NG_033191.1:g.69957_69959delinsCTG
NG_033191.2:g.69957_69959delinsCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.6327_6328+1delinsCTG
ENST00000399397.6:c.6291_6292+1delinsCTG
ENST00000342528.2:c.3345_3346+1delinsCTG
ENST00000399391.6:c.6327_6328+1delinsCTG
ENST00000399397.5:c.6291_6292+1delinsCTG
NM_001277269.1:c.6327_6328+1delinsCTG
NM_001292063.1:c.6291_6292+1delinsCTG
NM_001277269.2:c.6327_6328+1delinsCTG
NM_001292063.2:c.6291_6292+1delinsCTG