Canonical Allele Identifier: CA2576698812

Gene: OTOF

Linked Data

• gnomAD v4: 2-26461807-TGAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26461810_26461812del , CM000664.2:g.26461810_26461812del	GRCh38
NC_000002.11:g.26684678_26684680del , CM000664.1:g.26684678_26684680del	GRCh37
NC_000002.10:g.26538182_26538184del	NCBI36
NG_009937.1:g.101889_101891del

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.5419_5421del MANE Select	ENSP00000272371.2:p.Val1807del
ENST00000339598.8:c.3118_3120del MANE Plus Clinical	ENSP00000344521.3:p.Val1040del
ENST00000402415.8:c.3178_3180del	ENSP00000383906.4:p.Val1060del
ENST00000272371.6:c.5419_5421del	ENSP00000272371.2:p.Val1807del
ENST00000338581.10:c.3118_3120del	ENSP00000345137.6:p.Val1040del
ENST00000339598.7:c.3118_3120del	ENSP00000344521.3:p.Val1040del
ENST00000402415.7:c.3349_3351del	ENSP00000383906.3:p.Val1117del
ENST00000403946.7:c.5419_5421del	ENSP00000385255.3:p.Val1807del
NM_001287489.1:c.5419_5421del	NP_001274418.1:p.Val1807del
NM_004802.3:c.3118_3120del	NP_004793.2:p.Val1040del
NM_194248.2:c.5419_5421del	NP_919224.1:p.Val1807del
NM_194322.2:c.3349_3351del	NP_919303.1:p.Val1117del
NM_194323.2:c.3118_3120del	NP_919304.1:p.Val1040del
XM_005264644.2:c.5404_5406del	XP_005264701.1:p.Val1802del
XM_011533185.1:c.5464_5466del	XP_011531487.1:p.Val1822del
XM_017005338.1:c.5359_5361del	XP_016860827.1:p.Val1787del
NM_001287489.2:c.5419_5421del	NP_001274418.1:p.Val1807del
NM_004802.4:c.3118_3120del	NP_004793.2:p.Val1040del
NM_194248.3:c.5419_5421del MANE Select	NP_919224.1:p.Val1807del
NM_194322.3:c.3349_3351del	NP_919303.1:p.Val1117del
NM_194323.3:c.3118_3120del MANE Plus Clinical	NP_919304.1:p.Val1040del