Canonical Allele Identifier: CA1239829426

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482776_26482780delinsCGCGT , CM000664.2:g.26482776_26482780delinsCGCGT	GRCh38
NC_000002.11:g.26705644_26705648delinsCGCGT , CM000664.1:g.26705644_26705648delinsCGCGT	GRCh37
NC_000002.10:g.26559148_26559152delinsCGCGT	NCBI36
NG_009937.1:g.80919_80923delinsACGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-188_1393-184delinsACGCG MANE Select	ENSP00000272371.2:n.1393-188_1393-184delinsACGCG
ENST00000272371.6:c.1393-188_1393-184delinsACGCG	ENSP00000272371.2:n.1393-188_1393-184delinsACGCG
ENST00000403946.7:c.1393-188_1393-184delinsACGCG	ENSP00000385255.3:n.1393-188_1393-184delinsACGCG
NM_001287489.1:c.1393-188_1393-184delinsACGCG	NP_001274418.1:n.1393-188_1393-184delinsACGCG
NM_194248.2:c.1393-188_1393-184delinsACGCG	NP_919224.1:n.1393-188_1393-184delinsACGCG
XM_005264644.2:c.1438-188_1438-184delinsACGCG	XP_005264701.1:n.1438-188_1438-184delinsACGCG
XM_011533185.1:c.1438-188_1438-184delinsACGCG	XP_011531487.1:n.1438-188_1438-184delinsACGCG
XM_017005338.1:c.1393-188_1393-184delinsACGCG	XP_016860827.1:n.1393-188_1393-184delinsACGCG
NM_001287489.2:c.1393-188_1393-184delinsACGCG	NP_001274418.1:n.1393-188_1393-184delinsACGCG
NM_194248.3:c.1393-188_1393-184delinsACGCG MANE Select	NP_919224.1:n.1393-188_1393-184delinsACGCG