Canonical Allele Identifier: CA645517907

Gene: OTOF

Linked Data

• COSMIC: COSM6196389 ; COSM6196390 ; COSM6196391

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26477257_26477271del , CM000664.2:g.26477257_26477271del	GRCh38
NC_000002.11:g.26700125_26700139del , CM000664.1:g.26700125_26700139del	GRCh37
NC_000002.10:g.26553629_26553643del	NCBI36
NG_009937.1:g.86432_86446del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.2428_2442del MANE Select	ENSP00000272371.2:p.Arg810_Ala814del
ENST00000339598.8:c.187_201del MANE Plus Clinical	ENSP00000344521.3:p.Arg63_Ala67del
ENST00000402415.8:c.187_201del	ENSP00000383906.4:p.Arg63_Ala67del
ENST00000272371.6:c.2428_2442del	ENSP00000272371.2:p.Arg810_Ala814del
ENST00000338581.10:c.187_201del	ENSP00000345137.6:p.Arg63_Ala67del
ENST00000339598.7:c.187_201del	ENSP00000344521.3:p.Arg63_Ala67del
ENST00000402415.7:c.358_372del	ENSP00000383906.3:p.Arg120_Ala124del
ENST00000403946.7:c.2428_2442del	ENSP00000385255.3:p.Arg810_Ala814del
NM_001287489.1:c.2428_2442del	NP_001274418.1:p.Arg810_Ala814del
NM_004802.3:c.187_201del	NP_004793.2:p.Arg63_Ala67del
NM_194248.2:c.2428_2442del	NP_919224.1:p.Arg810_Ala814del
NM_194322.2:c.358_372del	NP_919303.1:p.Arg120_Ala124del
NM_194323.2:c.187_201del	NP_919304.1:p.Arg63_Ala67del
XM_005264644.2:c.2473_2487del	XP_005264701.1:p.Arg825_Ala829del
XM_011533185.1:c.2473_2487del	XP_011531487.1:p.Arg825_Ala829del
XM_017005338.1:c.2428_2442del	XP_016860827.1:p.Arg810_Ala814del
NM_001287489.2:c.2428_2442del	NP_001274418.1:p.Arg810_Ala814del
NM_004802.4:c.187_201del	NP_004793.2:p.Arg63_Ala67del
NM_194248.3:c.2428_2442del MANE Select	NP_919224.1:p.Arg810_Ala814del
NM_194322.3:c.358_372del	NP_919303.1:p.Arg120_Ala124del
NM_194323.3:c.187_201del MANE Plus Clinical	NP_919304.1:p.Arg63_Ala67del