Canonical Allele Identifier: CA646579948

Gene: OTOF

Linked Data

• COSMIC: COSN18726871 ; COSN18726875

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26458002_26458003insA , CM000664.2:g.26458002_26458003insA	GRCh38
NC_000002.11:g.26680870_26680871insA , CM000664.1:g.26680870_26680871insA	GRCh37
NC_000002.10:g.26534374_26534375insA	NCBI36
NG_009937.1:g.105696_105697insT
NG_042824.1:g.61091_61092insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.*235_*236insT MANE Select	ENSP00000272371.2:n.*235_*236insT
ENST00000339598.8:c.*37_*38insT MANE Plus Clinical	ENSP00000344521.3:n.*37_*38insT
ENST00000402415.8:c.*235_*236insT	ENSP00000383906.4:n.*235_*236insT
ENST00000272371.6:c.*235_*236insT	ENSP00000272371.2:n.*235_*236insT
ENST00000338581.10:c.*235_*236insT	ENSP00000345137.6:n.*235_*236insT
ENST00000339598.7:c.*37_*38insT	ENSP00000344521.3:n.*37_*38insT
ENST00000402415.7:c.*235_*236insT	ENSP00000383906.3:n.*235_*236insT
ENST00000403946.7:c.*37_*38insT	ENSP00000385255.3:n.*37_*38insT
NM_001287489.1:c.*37_*38insT	NP_001274418.1:n.*37_*38insT
NM_004802.3:c.*235_*236insT	NP_004793.2:n.*235_*236insT
NM_194248.2:c.*235_*236insT	NP_919224.1:n.*235_*236insT
NM_194322.2:c.*235_*236insT	NP_919303.1:n.*235_*236insT
NM_194323.2:c.*37_*38insT	NP_919304.1:n.*37_*38insT
XM_005264644.2:c.6016_6017insT	XP_005264701.1:n.6016_6017insT
XM_011533185.1:c.6076_6077insT	XP_011531487.1:n.6076_6077insT
NM_001287489.2:c.*37_*38insT	NP_001274418.1:n.*37_*38insT
NM_004802.4:c.*235_*236insT	NP_004793.2:n.*235_*236insT
NM_194248.3:c.*235_*236insT MANE Select	NP_919224.1:n.*235_*236insT
NM_194322.3:c.*235_*236insT	NP_919303.1:n.*235_*236insT
NM_194323.3:c.*37_*38insT MANE Plus Clinical	NP_919304.1:n.*37_*38insT