Canonical Allele Identifier: CA1239829479
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26482809_26482829delinsATGAGTGGGTGCATGTGTGCG , CM000664.2:g.26482809_26482829delinsATGAGTGGGTGCATGTGTGCG GRCh38
NC_000002.11:g.26705677_26705697delinsATGAGTGGGTGCATGTGTGCG , CM000664.1:g.26705677_26705697delinsATGAGTGGGTGCATGTGTGCG GRCh37
NC_000002.10:g.26559181_26559201delinsATGAGTGGGTGCATGTGTGCG NCBI36
NG_009937.1:g.80870_80890delinsCGCACACATGCACCCACTCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1393-237_1393-217delinsCGCACACATGCACCCACTCAT MANE Select ENSP00000272371.2:n.1393-237_1393-217delinsCGCACACATGCACCCACT...
ENST00000272371.6:c.1393-237_1393-217delinsCGCACACATGCACCCACTCAT ENSP00000272371.2:n.1393-237_1393-217delinsCGCACACATGCACCCACT...
ENST00000403946.7:c.1393-237_1393-217delinsCGCACACATGCACCCACTCAT ENSP00000385255.3:n.1393-237_1393-217delinsCGCACACATGCACCCACT...
NM_001287489.1:c.1393-237_1393-217delinsCGCACACATGCACCCACTCAT NP_001274418.1:n.1393-237_1393-217delinsCGCACACATGCACCCACTCAT...
NM_194248.2:c.1393-237_1393-217delinsCGCACACATGCACCCACTCAT NP_919224.1:n.1393-237_1393-217delinsCGCACACATGCACCCACTCAT
XM_005264644.2:c.1438-237_1438-217delinsCGCACACATGCACCCACTCAT XP_005264701.1:n.1438-237_1438-217delinsCGCACACATGCACCCACTCAT...
XM_011533185.1:c.1438-237_1438-217delinsCGCACACATGCACCCACTCAT XP_011531487.1:n.1438-237_1438-217delinsCGCACACATGCACCCACTCAT...
XM_017005338.1:c.1393-237_1393-217delinsCGCACACATGCACCCACTCAT XP_016860827.1:n.1393-237_1393-217delinsCGCACACATGCACCCACTCAT...
NM_001287489.2:c.1393-237_1393-217delinsCGCACACATGCACCCACTCAT NP_001274418.1:n.1393-237_1393-217delinsCGCACACATGCACCCACTCAT...
NM_194248.3:c.1393-237_1393-217delinsCGCACACATGCACCCACTCAT MANE Select NP_919224.1:n.1393-237_1393-217delinsCGCACACATGCACCCACTCAT