Canonical Allele Identifier: CA2840398264

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26460060dup , CM000664.2:g.26460060dup	GRCh38
NC_000002.11:g.26682928dup , CM000664.1:g.26682928dup	GRCh37
NC_000002.10:g.26536432dup	NCBI36
NG_009937.1:g.103640dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.5960dup MANE Select	ENSP00000272371.2:p.Gly1988TrpfsTer?
ENST00000339598.8:c.3512+588dup MANE Plus Clinical	ENSP00000344521.3:n.3512+588dup
ENST00000402415.8:c.3719dup	ENSP00000383906.4:p.Gly1241TrpfsTer?
ENST00000272371.6:c.5960dup	ENSP00000272371.2:p.Gly1988TrpfsTer?
ENST00000338581.10:c.3659dup	ENSP00000345137.6:p.Gly1221TrpfsTer?
ENST00000339598.7:c.3512+588dup	ENSP00000344521.3:n.3512+588dup
ENST00000402415.7:c.3890dup	ENSP00000383906.3:p.Gly1298TrpfsTer?
ENST00000403946.7:c.5813+588dup	ENSP00000385255.3:n.5813+588dup
NM_001287489.1:c.5813+588dup	NP_001274418.1:n.5813+588dup
NM_004802.3:c.3659dup	NP_004793.2:p.Gly1221TrpfsTer?
NM_194248.2:c.5960dup	NP_919224.1:p.Gly1988TrpfsTer?
NM_194322.2:c.3890dup	NP_919303.1:p.Gly1298TrpfsTer?
NM_194323.2:c.3512+588dup	NP_919304.1:n.3512+588dup
XM_005264644.2:c.5798+588dup	XP_005264701.1:n.5798+588dup
XM_011533185.1:c.5858+588dup	XP_011531487.1:n.5858+588dup
XM_017005338.1:c.5900dup	XP_016860827.1:p.Gly1968TrpfsTer?
NM_001287489.2:c.5813+588dup	NP_001274418.1:n.5813+588dup
NM_004802.4:c.3659dup	NP_004793.2:p.Gly1221TrpfsTer?
NM_194248.3:c.5960dup MANE Select	NP_919224.1:p.Gly1988TrpfsTer?
NM_194322.3:c.3890dup	NP_919303.1:p.Gly1298TrpfsTer?
NM_194323.3:c.3512+588dup MANE Plus Clinical	NP_919304.1:n.3512+588dup