Canonical Allele Identifier: CA1239829422

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482772_26482778delinsGGTGCGC , CM000664.2:g.26482772_26482778delinsGGTGCGC	GRCh38
NC_000002.11:g.26705640_26705646delinsGGTGCGC , CM000664.1:g.26705640_26705646delinsGGTGCGC	GRCh37
NC_000002.10:g.26559144_26559150delinsGGTGCGC	NCBI36
NG_009937.1:g.80921_80927delinsGCGCACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-186_1393-180delinsGCGCACC MANE Select	ENSP00000272371.2:n.1393-186_1393-180delinsGCGCACC
ENST00000272371.6:c.1393-186_1393-180delinsGCGCACC	ENSP00000272371.2:n.1393-186_1393-180delinsGCGCACC
ENST00000403946.7:c.1393-186_1393-180delinsGCGCACC	ENSP00000385255.3:n.1393-186_1393-180delinsGCGCACC
NM_001287489.1:c.1393-186_1393-180delinsGCGCACC	NP_001274418.1:n.1393-186_1393-180delinsGCGCACC
NM_194248.2:c.1393-186_1393-180delinsGCGCACC	NP_919224.1:n.1393-186_1393-180delinsGCGCACC
XM_005264644.2:c.1438-186_1438-180delinsGCGCACC	XP_005264701.1:n.1438-186_1438-180delinsGCGCACC
XM_011533185.1:c.1438-186_1438-180delinsGCGCACC	XP_011531487.1:n.1438-186_1438-180delinsGCGCACC
XM_017005338.1:c.1393-186_1393-180delinsGCGCACC	XP_016860827.1:n.1393-186_1393-180delinsGCGCACC
NM_001287489.2:c.1393-186_1393-180delinsGCGCACC	NP_001274418.1:n.1393-186_1393-180delinsGCGCACC
NM_194248.3:c.1393-186_1393-180delinsGCGCACC MANE Select	NP_919224.1:n.1393-186_1393-180delinsGCGCACC