Canonical Allele Identifier: CA2586968801

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467455_26467464del , CM000664.2:g.26467455_26467464del	GRCh38
NC_000002.11:g.26690323_26690332del , CM000664.1:g.26690323_26690332del	GRCh37
NC_000002.10:g.26543827_26543836del	NCBI36
NG_009937.1:g.96236_96245del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4129_4138del MANE Select	ENSP00000272371.2:p.Ala1377ArgfsTer?
ENST00000339598.8:c.1828_1837del MANE Plus Clinical	ENSP00000344521.3:p.Ala610ArgfsTer?
ENST00000402415.8:c.1888_1897del	ENSP00000383906.4:p.Ala630ArgfsTer?
ENST00000272371.6:c.4129_4138del	ENSP00000272371.2:p.Ala1377ArgfsTer?
ENST00000338581.10:c.1828_1837del	ENSP00000345137.6:p.Ala610ArgfsTer?
ENST00000339598.7:c.1828_1837del	ENSP00000344521.3:p.Ala610ArgfsTer?
ENST00000402415.7:c.2059_2068del	ENSP00000383906.3:p.Ala687ArgfsTer?
ENST00000403946.7:c.4129_4138del	ENSP00000385255.3:p.Ala1377ArgfsTer?
NM_001287489.1:c.4129_4138del	NP_001274418.1:p.Ala1377ArgfsTer?
NM_004802.3:c.1828_1837del	NP_004793.2:p.Ala610ArgfsTer?
NM_194248.2:c.4129_4138del	NP_919224.1:p.Ala1377ArgfsTer?
NM_194322.2:c.2059_2068del	NP_919303.1:p.Ala687ArgfsTer?
NM_194323.2:c.1828_1837del	NP_919304.1:p.Ala610ArgfsTer?
XM_005264644.2:c.4114_4123del	XP_005264701.1:p.Ala1372ArgfsTer?
XM_011533185.1:c.4174_4183del	XP_011531487.1:p.Ala1392ArgfsTer?
XM_017005338.1:c.4069_4078del	XP_016860827.1:p.Ala1357ArgfsTer?
NM_001287489.2:c.4129_4138del	NP_001274418.1:p.Ala1377ArgfsTer?
NM_004802.4:c.1828_1837del	NP_004793.2:p.Ala610ArgfsTer?
NM_194248.3:c.4129_4138del MANE Select	NP_919224.1:p.Ala1377ArgfsTer?
NM_194322.3:c.2059_2068del	NP_919303.1:p.Ala687ArgfsTer?
NM_194323.3:c.1828_1837del MANE Plus Clinical	NP_919304.1:p.Ala610ArgfsTer?