Canonical Allele Identifier: CA2658239228

Gene: OTOF

Linked Data

• gnomAD v4: 2-26483387-G-GGCAGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26483389_26483390insAGCTGC , CM000664.2:g.26483389_26483390insAGCTGC	GRCh38
NC_000002.11:g.26706257_26706258insAGCTGC , CM000664.1:g.26706257_26706258insAGCTGC	GRCh37
NC_000002.10:g.26559761_26559762insAGCTGC	NCBI36
NG_009937.1:g.80311_80312insAGCTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1392+74_1392+75insAGCTGC MANE Select	ENSP00000272371.2:n.1392+74_1392+75insAGCTGC
ENST00000272371.6:c.1392+74_1392+75insAGCTGC	ENSP00000272371.2:n.1392+74_1392+75insAGCTGC
ENST00000403946.7:c.1392+74_1392+75insAGCTGC	ENSP00000385255.3:n.1392+74_1392+75insAGCTGC
NM_001287489.1:c.1392+74_1392+75insAGCTGC	NP_001274418.1:n.1392+74_1392+75insAGCTGC
NM_194248.2:c.1392+74_1392+75insAGCTGC	NP_919224.1:n.1392+74_1392+75insAGCTGC
XM_005264644.2:c.1437+74_1437+75insAGCTGC	XP_005264701.1:n.1437+74_1437+75insAGCTGC
XM_011533185.1:c.1437+74_1437+75insAGCTGC	XP_011531487.1:n.1437+74_1437+75insAGCTGC
XM_017005338.1:c.1392+74_1392+75insAGCTGC	XP_016860827.1:n.1392+74_1392+75insAGCTGC
NM_001287489.2:c.1392+74_1392+75insAGCTGC	NP_001274418.1:n.1392+74_1392+75insAGCTGC
NM_194248.3:c.1392+74_1392+75insAGCTGC MANE Select	NP_919224.1:n.1392+74_1392+75insAGCTGC