Canonical Allele Identifier: CA2658232662

Gene: OTOF

Linked Data

• gnomAD v4: 2-26460125-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26460126del , CM000664.2:g.26460126del	GRCh38
NC_000002.11:g.26682994del , CM000664.1:g.26682994del	GRCh37
NC_000002.10:g.26536498del	NCBI36
NG_009937.1:g.103573del

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.5893del MANE Select	ENSP00000272371.2:p.Leu1965CysfsTer?
ENST00000339598.8:c.3512+521del MANE Plus Clinical	ENSP00000344521.3:n.3512+521del
ENST00000402415.8:c.3652del	ENSP00000383906.4:p.Leu1218CysfsTer?
ENST00000272371.6:c.5893del	ENSP00000272371.2:p.Leu1965CysfsTer?
ENST00000338581.10:c.3592del	ENSP00000345137.6:p.Leu1198CysfsTer?
ENST00000339598.7:c.3512+521del	ENSP00000344521.3:n.3512+521del
ENST00000402415.7:c.3823del	ENSP00000383906.3:p.Leu1275CysfsTer?
ENST00000403946.7:c.5813+521del	ENSP00000385255.3:n.5813+521del
NM_001287489.1:c.5813+521del	NP_001274418.1:n.5813+521del
NM_004802.3:c.3592del	NP_004793.2:p.Leu1198CysfsTer?
NM_194248.2:c.5893del	NP_919224.1:p.Leu1965CysfsTer?
NM_194322.2:c.3823del	NP_919303.1:p.Leu1275CysfsTer?
NM_194323.2:c.3512+521del	NP_919304.1:n.3512+521del
XM_005264644.2:c.5798+521del	XP_005264701.1:n.5798+521del
XM_011533185.1:c.5858+521del	XP_011531487.1:n.5858+521del
XM_017005338.1:c.5833del	XP_016860827.1:p.Leu1945CysfsTer?
NM_001287489.2:c.5813+521del	NP_001274418.1:n.5813+521del
NM_004802.4:c.3592del	NP_004793.2:p.Leu1198CysfsTer?
NM_194248.3:c.5893del MANE Select	NP_919224.1:p.Leu1965CysfsTer?
NM_194322.3:c.3823del	NP_919303.1:p.Leu1275CysfsTer?
NM_194323.3:c.3512+521del MANE Plus Clinical	NP_919304.1:n.3512+521del