Canonical Allele Identifier: CA2658240107

Gene: OTOF

Linked Data

• gnomAD v4: 2-26484723-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26484723_26484724insG , CM000664.2:g.26484723_26484724insG	GRCh38
NC_000002.11:g.26707591_26707592insG , CM000664.1:g.26707591_26707592insG	GRCh37
NC_000002.10:g.26561095_26561096insG	NCBI36
NG_009937.1:g.78975_78976insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1046-91_1046-90insC MANE Select	ENSP00000272371.2:n.1046-91_1046-90insC
ENST00000272371.6:c.1046-91_1046-90insC	ENSP00000272371.2:n.1046-91_1046-90insC
ENST00000403946.7:c.1046-91_1046-90insC	ENSP00000385255.3:n.1046-91_1046-90insC
NM_001287489.1:c.1046-91_1046-90insC	NP_001274418.1:n.1046-91_1046-90insC
NM_194248.2:c.1046-91_1046-90insC	NP_919224.1:n.1046-91_1046-90insC
XM_005264644.2:c.1091-91_1091-90insC	XP_005264701.1:n.1091-91_1091-90insC
XM_011533185.1:c.1091-91_1091-90insC	XP_011531487.1:n.1091-91_1091-90insC
XM_017005338.1:c.1046-91_1046-90insC	XP_016860827.1:n.1046-91_1046-90insC
NM_001287489.2:c.1046-91_1046-90insC	NP_001274418.1:n.1046-91_1046-90insC
NM_194248.3:c.1046-91_1046-90insC MANE Select	NP_919224.1:n.1046-91_1046-90insC