Canonical Allele Identifier: CA2749240873

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26484668_26484669insA , CM000664.2:g.26484668_26484669insA	GRCh38
NC_000002.11:g.26707536_26707537insA , CM000664.1:g.26707536_26707537insA	GRCh37
NC_000002.10:g.26561040_26561041insA	NCBI36
NG_009937.1:g.79030_79031insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1046-36_1046-35insT MANE Select	ENSP00000272371.2:n.1046-36_1046-35insT
ENST00000272371.6:c.1046-36_1046-35insT	ENSP00000272371.2:n.1046-36_1046-35insT
ENST00000403946.7:c.1046-36_1046-35insT	ENSP00000385255.3:n.1046-36_1046-35insT
NM_001287489.1:c.1046-36_1046-35insT	NP_001274418.1:n.1046-36_1046-35insT
NM_194248.2:c.1046-36_1046-35insT	NP_919224.1:n.1046-36_1046-35insT
XM_005264644.2:c.1091-36_1091-35insT	XP_005264701.1:n.1091-36_1091-35insT
XM_011533185.1:c.1091-36_1091-35insT	XP_011531487.1:n.1091-36_1091-35insT
XM_017005338.1:c.1046-36_1046-35insT	XP_016860827.1:n.1046-36_1046-35insT
NM_001287489.2:c.1046-36_1046-35insT	NP_001274418.1:n.1046-36_1046-35insT
NM_194248.3:c.1046-36_1046-35insT MANE Select	NP_919224.1:n.1046-36_1046-35insT