Canonical Allele Identifier: CA2658238906

Gene: OTOF

Linked Data

• gnomAD v4: 2-26482658-T-TGA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482659_26482660insAG , CM000664.2:g.26482659_26482660insAG	GRCh38
NC_000002.11:g.26705527_26705528insAG , CM000664.1:g.26705527_26705528insAG	GRCh37
NC_000002.10:g.26559031_26559032insAG	NCBI36
NG_009937.1:g.81040_81041insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-67_1393-66insTC MANE Select	ENSP00000272371.2:n.1393-67_1393-66insTC
ENST00000272371.6:c.1393-67_1393-66insTC	ENSP00000272371.2:n.1393-67_1393-66insTC
ENST00000403946.7:c.1393-67_1393-66insTC	ENSP00000385255.3:n.1393-67_1393-66insTC
NM_001287489.1:c.1393-67_1393-66insTC	NP_001274418.1:n.1393-67_1393-66insTC
NM_194248.2:c.1393-67_1393-66insTC	NP_919224.1:n.1393-67_1393-66insTC
XM_005264644.2:c.1438-67_1438-66insTC	XP_005264701.1:n.1438-67_1438-66insTC
XM_011533185.1:c.1438-67_1438-66insTC	XP_011531487.1:n.1438-67_1438-66insTC
XM_017005338.1:c.1393-67_1393-66insTC	XP_016860827.1:n.1393-67_1393-66insTC
NM_001287489.2:c.1393-67_1393-66insTC	NP_001274418.1:n.1393-67_1393-66insTC
NM_194248.3:c.1393-67_1393-66insTC MANE Select	NP_919224.1:n.1393-67_1393-66insTC