Canonical Allele Identifier: CA1239829390

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482745_26482761delinsGTGTGTGAGTGGGTGCA , CM000664.2:g.26482745_26482761delinsGTGTGTGAGTGGGTGCA	GRCh38
NC_000002.11:g.26705613_26705629delinsGTGTGTGAGTGGGTGCA , CM000664.1:g.26705613_26705629delinsGTGTGTGAGTGGGTGCA	GRCh37
NC_000002.10:g.26559117_26559133delinsGTGTGTGAGTGGGTGCA	NCBI36
NG_009937.1:g.80938_80954delinsTGCACCCACTCACACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-169_1393-153delinsTGCACCCACTCACACAC MANE Select	ENSP00000272371.2:n.1393-169_1393-153delinsTGCACCCACTCACACAC
ENST00000272371.6:c.1393-169_1393-153delinsTGCACCCACTCACACAC	ENSP00000272371.2:n.1393-169_1393-153delinsTGCACCCACTCACACAC
ENST00000403946.7:c.1393-169_1393-153delinsTGCACCCACTCACACAC	ENSP00000385255.3:n.1393-169_1393-153delinsTGCACCCACTCACACAC
NM_001287489.1:c.1393-169_1393-153delinsTGCACCCACTCACACAC	NP_001274418.1:n.1393-169_1393-153delinsTGCACCCACTCACACAC
NM_194248.2:c.1393-169_1393-153delinsTGCACCCACTCACACAC	NP_919224.1:n.1393-169_1393-153delinsTGCACCCACTCACACAC
XM_005264644.2:c.1438-169_1438-153delinsTGCACCCACTCACACAC	XP_005264701.1:n.1438-169_1438-153delinsTGCACCCACTCACACAC
XM_011533185.1:c.1438-169_1438-153delinsTGCACCCACTCACACAC	XP_011531487.1:n.1438-169_1438-153delinsTGCACCCACTCACACAC
XM_017005338.1:c.1393-169_1393-153delinsTGCACCCACTCACACAC	XP_016860827.1:n.1393-169_1393-153delinsTGCACCCACTCACACAC
NM_001287489.2:c.1393-169_1393-153delinsTGCACCCACTCACACAC	NP_001274418.1:n.1393-169_1393-153delinsTGCACCCACTCACACAC
NM_194248.3:c.1393-169_1393-153delinsTGCACCCACTCACACAC MANE Select	NP_919224.1:n.1393-169_1393-153delinsTGCACCCACTCACACAC