Canonical Allele Identifier: CA1239829462
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26482799_26482803delinsATGTG , CM000664.2:g.26482799_26482803delinsATGTG GRCh38
NC_000002.11:g.26705667_26705671delinsATGTG , CM000664.1:g.26705667_26705671delinsATGTG GRCh37
NC_000002.10:g.26559171_26559175delinsATGTG NCBI36
NG_009937.1:g.80896_80900delinsCACAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1393-211_1393-207delinsCACAT MANE Select ENSP00000272371.2:n.1393-211_1393-207delinsCACAT
ENST00000272371.6:c.1393-211_1393-207delinsCACAT ENSP00000272371.2:n.1393-211_1393-207delinsCACAT
ENST00000403946.7:c.1393-211_1393-207delinsCACAT ENSP00000385255.3:n.1393-211_1393-207delinsCACAT
NM_001287489.1:c.1393-211_1393-207delinsCACAT NP_001274418.1:n.1393-211_1393-207delinsCACAT
NM_194248.2:c.1393-211_1393-207delinsCACAT NP_919224.1:n.1393-211_1393-207delinsCACAT
XM_005264644.2:c.1438-211_1438-207delinsCACAT XP_005264701.1:n.1438-211_1438-207delinsCACAT
XM_011533185.1:c.1438-211_1438-207delinsCACAT XP_011531487.1:n.1438-211_1438-207delinsCACAT
XM_017005338.1:c.1393-211_1393-207delinsCACAT XP_016860827.1:n.1393-211_1393-207delinsCACAT
NM_001287489.2:c.1393-211_1393-207delinsCACAT NP_001274418.1:n.1393-211_1393-207delinsCACAT
NM_194248.3:c.1393-211_1393-207delinsCACAT MANE Select NP_919224.1:n.1393-211_1393-207delinsCACAT