Canonical Allele Identifier: CA2576699132

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467395_26467397dup , CM000664.2:g.26467395_26467397dup	GRCh38
NC_000002.11:g.26690263_26690265dup , CM000664.1:g.26690263_26690265dup	GRCh37
NC_000002.10:g.26543767_26543769dup	NCBI36
NG_009937.1:g.96302_96304dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4195_4197dup MANE Select	ENSP00000272371.2:p.Glu1399_Lys1400insGlu
ENST00000339598.8:c.1894_1896dup MANE Plus Clinical	ENSP00000344521.3:p.Glu632_Lys633insGlu
ENST00000402415.8:c.1954_1956dup	ENSP00000383906.4:p.Glu652_Lys653insGlu
ENST00000272371.6:c.4195_4197dup	ENSP00000272371.2:p.Glu1399_Lys1400insGlu
ENST00000338581.10:c.1894_1896dup	ENSP00000345137.6:p.Glu632_Lys633insGlu
ENST00000339598.7:c.1894_1896dup	ENSP00000344521.3:p.Glu632_Lys633insGlu
ENST00000402415.7:c.2125_2127dup	ENSP00000383906.3:p.Glu709_Lys710insGlu
ENST00000403946.7:c.4195_4197dup	ENSP00000385255.3:p.Glu1399_Lys1400insGlu
NM_001287489.1:c.4195_4197dup	NP_001274418.1:p.Glu1399_Lys1400insGlu
NM_004802.3:c.1894_1896dup	NP_004793.2:p.Glu632_Lys633insGlu
NM_194248.2:c.4195_4197dup	NP_919224.1:p.Glu1399_Lys1400insGlu
NM_194322.2:c.2125_2127dup	NP_919303.1:p.Glu709_Lys710insGlu
NM_194323.2:c.1894_1896dup	NP_919304.1:p.Glu632_Lys633insGlu
XM_005264644.2:c.4180_4182dup	XP_005264701.1:p.Glu1394_Lys1395insGlu
XM_011533185.1:c.4240_4242dup	XP_011531487.1:p.Glu1414_Lys1415insGlu
XM_017005338.1:c.4135_4137dup	XP_016860827.1:p.Glu1379_Lys1380insGlu
NM_001287489.2:c.4195_4197dup	NP_001274418.1:p.Glu1399_Lys1400insGlu
NM_004802.4:c.1894_1896dup	NP_004793.2:p.Glu632_Lys633insGlu
NM_194248.3:c.4195_4197dup MANE Select	NP_919224.1:p.Glu1399_Lys1400insGlu
NM_194322.3:c.2125_2127dup	NP_919303.1:p.Glu709_Lys710insGlu
NM_194323.3:c.1894_1896dup MANE Plus Clinical	NP_919304.1:p.Glu632_Lys633insGlu