Canonical Allele Identifier: CA2658232651

Gene: OTOF

Linked Data

• gnomAD v4: 2-26461798-TCTTGGAGATGACGATCTTCTCCTCCGCCGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26461800_26461829del , CM000664.2:g.26461800_26461829del	GRCh38
NC_000002.11:g.26684668_26684697del , CM000664.1:g.26684668_26684697del	GRCh37
NC_000002.10:g.26538172_26538201del	NCBI36
NG_009937.1:g.101871_101900del

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.5401_5430del MANE Select	ENSP00000272371.2:p.Ala1801_Lys1810del
ENST00000339598.8:c.3100_3129del MANE Plus Clinical	ENSP00000344521.3:p.Ala1034_Lys1043del
ENST00000402415.8:c.3160_3189del	ENSP00000383906.4:p.Ala1054_Lys1063del
ENST00000272371.6:c.5401_5430del	ENSP00000272371.2:p.Ala1801_Lys1810del
ENST00000338581.10:c.3100_3129del	ENSP00000345137.6:p.Ala1034_Lys1043del
ENST00000339598.7:c.3100_3129del	ENSP00000344521.3:p.Ala1034_Lys1043del
ENST00000402415.7:c.3331_3360del	ENSP00000383906.3:p.Ala1111_Lys1120del
ENST00000403946.7:c.5401_5430del	ENSP00000385255.3:p.Ala1801_Lys1810del
NM_001287489.1:c.5401_5430del	NP_001274418.1:p.Ala1801_Lys1810del
NM_004802.3:c.3100_3129del	NP_004793.2:p.Ala1034_Lys1043del
NM_194248.2:c.5401_5430del	NP_919224.1:p.Ala1801_Lys1810del
NM_194322.2:c.3331_3360del	NP_919303.1:p.Ala1111_Lys1120del
NM_194323.2:c.3100_3129del	NP_919304.1:p.Ala1034_Lys1043del
XM_005264644.2:c.5386_5415del	XP_005264701.1:p.Ala1796_Lys1805del
XM_011533185.1:c.5446_5475del	XP_011531487.1:p.Ala1816_Lys1825del
XM_017005338.1:c.5341_5370del	XP_016860827.1:p.Ala1781_Lys1790del
NM_001287489.2:c.5401_5430del	NP_001274418.1:p.Ala1801_Lys1810del
NM_004802.4:c.3100_3129del	NP_004793.2:p.Ala1034_Lys1043del
NM_194248.3:c.5401_5430del MANE Select	NP_919224.1:p.Ala1801_Lys1810del
NM_194322.3:c.3331_3360del	NP_919303.1:p.Ala1111_Lys1120del
NM_194323.3:c.3100_3129del MANE Plus Clinical	NP_919304.1:p.Ala1034_Lys1043del