Canonical Allele Identifier: CA2658234833

Gene: OTOF

Linked Data

• gnomAD v4: 2-26467271-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467271_26467272insA , CM000664.2:g.26467271_26467272insA	GRCh38
NC_000002.11:g.26690139_26690140insA , CM000664.1:g.26690139_26690140insA	GRCh37
NC_000002.10:g.26543643_26543644insA	NCBI36
NG_009937.1:g.96427_96428insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4228-39_4228-38insT MANE Select	ENSP00000272371.2:n.4228-39_4228-38insT
ENST00000339598.8:c.1927-39_1927-38insT MANE Plus Clinical	ENSP00000344521.3:n.1927-39_1927-38insT
ENST00000402415.8:c.1987-39_1987-38insT	ENSP00000383906.4:n.1987-39_1987-38insT
ENST00000272371.6:c.4228-39_4228-38insT	ENSP00000272371.2:n.4228-39_4228-38insT
ENST00000338581.10:c.1927-39_1927-38insT	ENSP00000345137.6:n.1927-39_1927-38insT
ENST00000339598.7:c.1927-39_1927-38insT	ENSP00000344521.3:n.1927-39_1927-38insT
ENST00000402415.7:c.2158-39_2158-38insT	ENSP00000383906.3:n.2158-39_2158-38insT
ENST00000403946.7:c.4228-39_4228-38insT	ENSP00000385255.3:n.4228-39_4228-38insT
NM_001287489.1:c.4228-39_4228-38insT	NP_001274418.1:n.4228-39_4228-38insT
NM_004802.3:c.1927-39_1927-38insT	NP_004793.2:n.1927-39_1927-38insT
NM_194248.2:c.4228-39_4228-38insT	NP_919224.1:n.4228-39_4228-38insT
NM_194322.2:c.2158-39_2158-38insT	NP_919303.1:n.2158-39_2158-38insT
NM_194323.2:c.1927-39_1927-38insT	NP_919304.1:n.1927-39_1927-38insT
XM_005264644.2:c.4213-39_4213-38insT	XP_005264701.1:n.4213-39_4213-38insT
XM_011533185.1:c.4273-39_4273-38insT	XP_011531487.1:n.4273-39_4273-38insT
XM_017005338.1:c.4168-39_4168-38insT	XP_016860827.1:n.4168-39_4168-38insT
NM_001287489.2:c.4228-39_4228-38insT	NP_001274418.1:n.4228-39_4228-38insT
NM_004802.4:c.1927-39_1927-38insT	NP_004793.2:n.1927-39_1927-38insT
NM_194248.3:c.4228-39_4228-38insT MANE Select	NP_919224.1:n.4228-39_4228-38insT
NM_194322.3:c.2158-39_2158-38insT	NP_919303.1:n.2158-39_2158-38insT
NM_194323.3:c.1927-39_1927-38insT MANE Plus Clinical	NP_919304.1:n.1927-39_1927-38insT