Canonical Allele Identifier: CA1239818503

Gene: OTOF

Linked Data

• dbSNP Id: rs778787323

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467448_26467450dup , CM000664.2:g.26467448_26467450dup	GRCh38
NC_000002.11:g.26690316_26690318dup , CM000664.1:g.26690316_26690318dup	GRCh37
NC_000002.10:g.26543820_26543822dup	NCBI36
NG_009937.1:g.96259_96261dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4152_4154dup MANE Select	ENSP00000272371.2:p.Lys1385_Thr1386insLys
ENST00000339598.8:c.1851_1853dup MANE Plus Clinical	ENSP00000344521.3:p.Lys618_Thr619insLys
ENST00000402415.8:c.1911_1913dup	ENSP00000383906.4:p.Lys638_Thr639insLys
ENST00000272371.6:c.4152_4154dup	ENSP00000272371.2:p.Lys1385_Thr1386insLys
ENST00000338581.10:c.1851_1853dup	ENSP00000345137.6:p.Lys618_Thr619insLys
ENST00000339598.7:c.1851_1853dup	ENSP00000344521.3:p.Lys618_Thr619insLys
ENST00000402415.7:c.2082_2084dup	ENSP00000383906.3:p.Lys695_Thr696insLys
ENST00000403946.7:c.4152_4154dup	ENSP00000385255.3:p.Lys1385_Thr1386insLys
NM_001287489.1:c.4152_4154dup	NP_001274418.1:p.Lys1385_Thr1386insLys
NM_004802.3:c.1851_1853dup	NP_004793.2:p.Lys618_Thr619insLys
NM_194248.2:c.4152_4154dup	NP_919224.1:p.Lys1385_Thr1386insLys
NM_194322.2:c.2082_2084dup	NP_919303.1:p.Lys695_Thr696insLys
NM_194323.2:c.1851_1853dup	NP_919304.1:p.Lys618_Thr619insLys
XM_005264644.2:c.4137_4139dup	XP_005264701.1:p.Lys1380_Thr1381insLys
XM_011533185.1:c.4197_4199dup	XP_011531487.1:p.Lys1400_Thr1401insLys
XM_017005338.1:c.4092_4094dup	XP_016860827.1:p.Lys1365_Thr1366insLys
NM_001287489.2:c.4152_4154dup	NP_001274418.1:p.Lys1385_Thr1386insLys
NM_004802.4:c.1851_1853dup	NP_004793.2:p.Lys618_Thr619insLys
NM_194248.3:c.4152_4154dup MANE Select	NP_919224.1:p.Lys1385_Thr1386insLys
NM_194322.3:c.2082_2084dup	NP_919303.1:p.Lys695_Thr696insLys
NM_194323.3:c.1851_1853dup MANE Plus Clinical	NP_919304.1:p.Lys618_Thr619insLys