Canonical Allele Identifier: CA2749240777
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26482682_26482701del , CM000664.2:g.26482682_26482701del GRCh38
NC_000002.11:g.26705550_26705569del , CM000664.1:g.26705550_26705569del GRCh37
NC_000002.10:g.26559054_26559073del NCBI36
NG_009937.1:g.81000_81019del

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1393-107_1393-88del MANE Select ENSP00000272371.2:n.1393-107_1393-88del
ENST00000272371.6:c.1393-107_1393-88del ENSP00000272371.2:n.1393-107_1393-88del
ENST00000403946.7:c.1393-107_1393-88del ENSP00000385255.3:n.1393-107_1393-88del
NM_001287489.1:c.1393-107_1393-88del NP_001274418.1:n.1393-107_1393-88del
NM_194248.2:c.1393-107_1393-88del NP_919224.1:n.1393-107_1393-88del
XM_005264644.2:c.1438-107_1438-88del XP_005264701.1:n.1438-107_1438-88del
XM_011533185.1:c.1438-107_1438-88del XP_011531487.1:n.1438-107_1438-88del
XM_017005338.1:c.1393-107_1393-88del XP_016860827.1:n.1393-107_1393-88del
NM_001287489.2:c.1393-107_1393-88del NP_001274418.1:n.1393-107_1393-88del
NM_194248.3:c.1393-107_1393-88del MANE Select NP_919224.1:n.1393-107_1393-88del