Canonical Allele Identifier: CA1239822013

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26457998_26458001delinsATGC , CM000664.2:g.26457998_26458001delinsATGC	GRCh38
NC_000002.11:g.26680866_26680869delinsATGC , CM000664.1:g.26680866_26680869delinsATGC	GRCh37
NC_000002.10:g.26534370_26534373delinsATGC	NCBI36
NG_009937.1:g.105698_105701delinsGCAT
NG_042824.1:g.61087_61090delinsATGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.*237_*240delinsGCAT MANE Select	ENSP00000272371.2:n.*237_*240delinsGCAT
ENST00000339598.8:c.*39_*42delinsGCAT MANE Plus Clinical	ENSP00000344521.3:n.*39_*42delinsGCAT
ENST00000402415.8:c.*237_*240delinsGCAT	ENSP00000383906.4:n.*237_*240delinsGCAT
ENST00000272371.6:c.*237_*240delinsGCAT	ENSP00000272371.2:n.*237_*240delinsGCAT
ENST00000338581.10:c.*237_*240delinsGCAT	ENSP00000345137.6:n.*237_*240delinsGCAT
ENST00000339598.7:c.*39_*42delinsGCAT	ENSP00000344521.3:n.*39_*42delinsGCAT
ENST00000402415.7:c.*237_*240delinsGCAT	ENSP00000383906.3:n.*237_*240delinsGCAT
ENST00000403946.7:c.*39_*42delinsGCAT	ENSP00000385255.3:n.*39_*42delinsGCAT
NM_001287489.1:c.*39_*42delinsGCAT	NP_001274418.1:n.*39_*42delinsGCAT
NM_004802.3:c.*237_*240delinsGCAT	NP_004793.2:n.*237_*240delinsGCAT
NM_194248.2:c.*237_*240delinsGCAT	NP_919224.1:n.*237_*240delinsGCAT
NM_194322.2:c.*237_*240delinsGCAT	NP_919303.1:n.*237_*240delinsGCAT
NM_194323.2:c.*39_*42delinsGCAT	NP_919304.1:n.*39_*42delinsGCAT
XM_005264644.2:c.6018_6021delinsGCAT	XP_005264701.1:n.6018_6021delinsGCAT
XM_011533185.1:c.6078_6081delinsGCAT	XP_011531487.1:n.6078_6081delinsGCAT
NM_001287489.2:c.*39_*42delinsGCAT	NP_001274418.1:n.*39_*42delinsGCAT
NM_004802.4:c.*237_*240delinsGCAT	NP_004793.2:n.*237_*240delinsGCAT
NM_194248.3:c.*237_*240delinsGCAT MANE Select	NP_919224.1:n.*237_*240delinsGCAT
NM_194322.3:c.*237_*240delinsGCAT	NP_919303.1:n.*237_*240delinsGCAT
NM_194323.3:c.*39_*42delinsGCAT MANE Plus Clinical	NP_919304.1:n.*39_*42delinsGCAT