Canonical Allele Identifier: CA2576699726
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26482660_26482665del , CM000664.2:g.26482660_26482665del GRCh38
NC_000002.11:g.26705528_26705533del , CM000664.1:g.26705528_26705533del GRCh37
NC_000002.10:g.26559032_26559037del NCBI36
NG_009937.1:g.81037_81042del

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1393-70_1393-65del MANE Select ENSP00000272371.2:n.1393-70_1393-65del
ENST00000272371.6:c.1393-70_1393-65del ENSP00000272371.2:n.1393-70_1393-65del
ENST00000403946.7:c.1393-70_1393-65del ENSP00000385255.3:n.1393-70_1393-65del
NM_001287489.1:c.1393-70_1393-65del NP_001274418.1:n.1393-70_1393-65del
NM_194248.2:c.1393-70_1393-65del NP_919224.1:n.1393-70_1393-65del
XM_005264644.2:c.1438-70_1438-65del XP_005264701.1:n.1438-70_1438-65del
XM_011533185.1:c.1438-70_1438-65del XP_011531487.1:n.1438-70_1438-65del
XM_017005338.1:c.1393-70_1393-65del XP_016860827.1:n.1393-70_1393-65del
NM_001287489.2:c.1393-70_1393-65del NP_001274418.1:n.1393-70_1393-65del
NM_194248.3:c.1393-70_1393-65del MANE Select NP_919224.1:n.1393-70_1393-65del