Canonical Allele Identifier: CA916496182

Gene: OTOF

Linked Data

• dbSNP Id: rs1553354202

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482576_26482577insTGCACTGAAGTCT , CM000664.2:g.26482576_26482577insTGCACTGAAGTCT	GRCh38
NC_000002.11:g.26705444_26705445insTGCACTGAAGTCT , CM000664.1:g.26705444_26705445insTGCACTGAAGTCT	GRCh37
NC_000002.10:g.26558948_26558949insTGCACTGAAGTCT	NCBI36
NG_009937.1:g.81125_81126insCTTCAGTGCAAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1411_1412insCTTCAGTGCAAGA MANE Select	ENSP00000272371.2:p.Lys471ThrfsTer9
ENST00000272371.6:c.1411_1412insCTTCAGTGCAAGA	ENSP00000272371.2:p.Lys471ThrfsTer9
ENST00000403946.7:c.1411_1412insCTTCAGTGCAAGA	ENSP00000385255.3:p.Lys471ThrfsTer9
NM_001287489.1:c.1411_1412insCTTCAGTGCAAGA	NP_001274418.1:p.Lys471ThrfsTer9
NM_194248.2:c.1411_1412insCTTCAGTGCAAGA	NP_919224.1:p.Lys471ThrfsTer9
XM_005264644.2:c.1456_1457insCTTCAGTGCAAGA	XP_005264701.1:p.Lys486ThrfsTer9
XM_011533185.1:c.1456_1457insCTTCAGTGCAAGA	XP_011531487.1:p.Lys486ThrfsTer9
XM_017005338.1:c.1411_1412insCTTCAGTGCAAGA	XP_016860827.1:p.Lys471ThrfsTer9
NM_001287489.2:c.1411_1412insCTTCAGTGCAAGA	NP_001274418.1:p.Lys471ThrfsTer9
NM_194248.3:c.1411_1412insCTTCAGTGCAAGA MANE Select	NP_919224.1:p.Lys471ThrfsTer9