Canonical Allele Identifier: CA2698918693

Gene: OTOF

Linked Data

• dbSNP Id: rs2148031254

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467461del , CM000664.2:g.26467461del	GRCh38
NC_000002.11:g.26690329del , CM000664.1:g.26690329del	GRCh37
NC_000002.10:g.26543833del	NCBI36
NG_009937.1:g.96238del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4131del MANE Select	ENSP00000272371.2:p.Ala1378ProfsTer?
ENST00000339598.8:c.1830del MANE Plus Clinical	ENSP00000344521.3:p.Ala611ProfsTer?
ENST00000402415.8:c.1890del	ENSP00000383906.4:p.Ala631ProfsTer?
ENST00000272371.6:c.4131del	ENSP00000272371.2:p.Ala1378ProfsTer?
ENST00000338581.10:c.1830del	ENSP00000345137.6:p.Ala611ProfsTer?
ENST00000339598.7:c.1830del	ENSP00000344521.3:p.Ala611ProfsTer?
ENST00000402415.7:c.2061del	ENSP00000383906.3:p.Ala688ProfsTer?
ENST00000403946.7:c.4131del	ENSP00000385255.3:p.Ala1378ProfsTer?
NM_001287489.1:c.4131del	NP_001274418.1:p.Ala1378ProfsTer?
NM_004802.3:c.1830del	NP_004793.2:p.Ala611ProfsTer?
NM_194248.2:c.4131del	NP_919224.1:p.Ala1378ProfsTer?
NM_194322.2:c.2061del	NP_919303.1:p.Ala688ProfsTer?
NM_194323.2:c.1830del	NP_919304.1:p.Ala611ProfsTer?
XM_005264644.2:c.4116del	XP_005264701.1:p.Ala1373ProfsTer?
XM_011533185.1:c.4176del	XP_011531487.1:p.Ala1393ProfsTer?
XM_017005338.1:c.4071del	XP_016860827.1:p.Ala1358ProfsTer?
NM_001287489.2:c.4131del	NP_001274418.1:p.Ala1378ProfsTer?
NM_004802.4:c.1830del	NP_004793.2:p.Ala611ProfsTer?
NM_194248.3:c.4131del MANE Select	NP_919224.1:p.Ala1378ProfsTer?
NM_194322.3:c.2061del	NP_919303.1:p.Ala688ProfsTer?
NM_194323.3:c.1830del MANE Plus Clinical	NP_919304.1:p.Ala611ProfsTer?