Canonical Allele Identifier: CA2749240778
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26482706_26482707del , CM000664.2:g.26482706_26482707del GRCh38
NC_000002.11:g.26705574_26705575del , CM000664.1:g.26705574_26705575del GRCh37
NC_000002.10:g.26559078_26559079del NCBI36
NG_009937.1:g.80993_80994del

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1393-114_1393-113del MANE Select ENSP00000272371.2:n.1393-114_1393-113del
ENST00000272371.6:c.1393-114_1393-113del ENSP00000272371.2:n.1393-114_1393-113del
ENST00000403946.7:c.1393-114_1393-113del ENSP00000385255.3:n.1393-114_1393-113del
NM_001287489.1:c.1393-114_1393-113del NP_001274418.1:n.1393-114_1393-113del
NM_194248.2:c.1393-114_1393-113del NP_919224.1:n.1393-114_1393-113del
XM_005264644.2:c.1438-114_1438-113del XP_005264701.1:n.1438-114_1438-113del
XM_011533185.1:c.1438-114_1438-113del XP_011531487.1:n.1438-114_1438-113del
XM_017005338.1:c.1393-114_1393-113del XP_016860827.1:n.1393-114_1393-113del
NM_001287489.2:c.1393-114_1393-113del NP_001274418.1:n.1393-114_1393-113del
NM_194248.3:c.1393-114_1393-113del MANE Select NP_919224.1:n.1393-114_1393-113del