Canonical Allele Identifier: CA2519265579

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26458008del , CM000664.2:g.26458008del	GRCh38
NC_000002.11:g.26680876del , CM000664.1:g.26680876del	GRCh37
NC_000002.10:g.26534380del	NCBI36
NG_009937.1:g.105693del
NG_042824.1:g.61097del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.*232del MANE Select	ENSP00000272371.2:n.*232del
ENST00000339598.8:c.*34del MANE Plus Clinical	ENSP00000344521.3:n.*34del
ENST00000402415.8:c.*232del	ENSP00000383906.4:n.*232del
ENST00000272371.6:c.*232del	ENSP00000272371.2:n.*232del
ENST00000338581.10:c.*232del	ENSP00000345137.6:n.*232del
ENST00000339598.7:c.*34del	ENSP00000344521.3:n.*34del
ENST00000402415.7:c.*232del	ENSP00000383906.3:n.*232del
ENST00000403946.7:c.*34del	ENSP00000385255.3:n.*34del
NM_001287489.1:c.*34del	NP_001274418.1:n.*34del
NM_004802.3:c.*232del	NP_004793.2:n.*232del
NM_194248.2:c.*232del	NP_919224.1:n.*232del
NM_194322.2:c.*232del	NP_919303.1:n.*232del
NM_194323.2:c.*34del	NP_919304.1:n.*34del
XM_005264644.2:c.6013del	XP_005264701.1:n.6013del
XM_011533185.1:c.6073del	XP_011531487.1:n.6073del
NM_001287489.2:c.*34del	NP_001274418.1:n.*34del
NM_004802.4:c.*232del	NP_004793.2:n.*232del
NM_194248.3:c.*232del MANE Select	NP_919224.1:n.*232del
NM_194322.3:c.*232del	NP_919303.1:n.*232del
NM_194323.3:c.*34del MANE Plus Clinical	NP_919304.1:n.*34del