Canonical Allele Identifier: CA2523588077
Gene: OTOF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26467126_26467143del , CM000664.2:g.26467126_26467143del GRCh38
NC_000002.11:g.26689994_26690011del , CM000664.1:g.26689994_26690011del GRCh37
NC_000002.10:g.26543498_26543515del NCBI36
NG_009937.1:g.96561_96578del

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.4323_4340del MANE Select ENSP00000272371.2:p.Asp1441_Glu1446del
ENST00000339598.8:c.2022_2039del MANE Plus Clinical ENSP00000344521.3:p.Asp674_Glu679del
ENST00000402415.8:c.2082_2099del ENSP00000383906.4:p.Asp694_Glu699del
ENST00000272371.6:c.4323_4340del ENSP00000272371.2:p.Asp1441_Glu1446del
ENST00000338581.10:c.2022_2039del ENSP00000345137.6:p.Asp674_Glu679del
ENST00000339598.7:c.2022_2039del ENSP00000344521.3:p.Asp674_Glu679del
ENST00000402415.7:c.2253_2270del ENSP00000383906.3:p.Asp751_Glu756del
ENST00000403946.7:c.4323_4340del ENSP00000385255.3:p.Asp1441_Glu1446del
NM_001287489.1:c.4323_4340del NP_001274418.1:p.Asp1441_Glu1446del
NM_004802.3:c.2022_2039del NP_004793.2:p.Asp674_Glu679del
NM_194248.2:c.4323_4340del NP_919224.1:p.Asp1441_Glu1446del
NM_194322.2:c.2253_2270del NP_919303.1:p.Asp751_Glu756del
NM_194323.2:c.2022_2039del NP_919304.1:p.Asp674_Glu679del
XM_005264644.2:c.4308_4325del XP_005264701.1:p.Asp1436_Glu1441del
XM_011533185.1:c.4368_4385del XP_011531487.1:p.Asp1456_Glu1461del
XM_017005338.1:c.4263_4280del XP_016860827.1:p.Asp1421_Glu1426del
NM_001287489.2:c.4323_4340del NP_001274418.1:p.Asp1441_Glu1446del
NM_004802.4:c.2022_2039del NP_004793.2:p.Asp674_Glu679del
NM_194248.3:c.4323_4340del MANE Select NP_919224.1:p.Asp1441_Glu1446del
NM_194322.3:c.2253_2270del NP_919303.1:p.Asp751_Glu756del
NM_194323.3:c.2022_2039del MANE Plus Clinical NP_919304.1:p.Asp674_Glu679del