Canonical Allele Identifier: CA2658237851
Gene: OTOF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26477218_26477223del , CM000664.2:g.26477218_26477223del GRCh38
NC_000002.11:g.26700086_26700091del , CM000664.1:g.26700086_26700091del GRCh37
NC_000002.10:g.26553590_26553595del NCBI36
NG_009937.1:g.86480_86485del

Transcript Alleles

HGVS Amino-acid change
ENST00000272371.7:c.2476_2481del MANE Select ENSP00000272371.2:p.Arg826_Leu827del
ENST00000339598.8:c.235_240del MANE Plus Clinical ENSP00000344521.3:p.Arg79_Leu80del
ENST00000402415.8:c.235_240del ENSP00000383906.4:p.Arg79_Leu80del
ENST00000272371.6:c.2476_2481del ENSP00000272371.2:p.Arg826_Leu827del
ENST00000338581.10:c.235_240del ENSP00000345137.6:p.Arg79_Leu80del
ENST00000339598.7:c.235_240del ENSP00000344521.3:p.Arg79_Leu80del
ENST00000402415.7:c.406_411del ENSP00000383906.3:p.Arg136_Leu137del
ENST00000403946.7:c.2476_2481del ENSP00000385255.3:p.Arg826_Leu827del
NM_001287489.1:c.2476_2481del NP_001274418.1:p.Arg826_Leu827del
NM_004802.3:c.235_240del NP_004793.2:p.Arg79_Leu80del
NM_194248.2:c.2476_2481del NP_919224.1:p.Arg826_Leu827del
NM_194322.2:c.406_411del NP_919303.1:p.Arg136_Leu137del
NM_194323.2:c.235_240del NP_919304.1:p.Arg79_Leu80del
XM_005264644.2:c.2521_2526del XP_005264701.1:p.Arg841_Leu842del
XM_011533185.1:c.2521_2526del XP_011531487.1:p.Arg841_Leu842del
XM_017005338.1:c.2476_2481del XP_016860827.1:p.Arg826_Leu827del
NM_001287489.2:c.2476_2481del NP_001274418.1:p.Arg826_Leu827del
NM_004802.4:c.235_240del NP_004793.2:p.Arg79_Leu80del
NM_194248.3:c.2476_2481del MANE Select NP_919224.1:p.Arg826_Leu827del
NM_194322.3:c.406_411del NP_919303.1:p.Arg136_Leu137del
NM_194323.3:c.235_240del MANE Plus Clinical NP_919304.1:p.Arg79_Leu80del