Canonical Allele Identifier: CA767290087

Gene: OTOF

Linked Data

• dbSNP Id: rs1485151499
• gnomAD v4: 2-26482665-G-GGGCGCGTGTGTGTGTGTGAGTT
• MyVariant Identifiers: chr2:g.26705533_26705534insGGCGCGTGTGTGTGTGTGAGTT (hg19) ; chr2:g.26482665_26482666insGGCGCGTGTGTGTGTGTGAGTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482670_26482671insGTGTGTGTGTGTGAGTTGGCGC , CM000664.2:g.26482670_26482671insGTGTGTGTGTGTGAGTTGGCGC	GRCh38
NC_000002.11:g.26705538_26705539insGTGTGTGTGTGTGAGTTGGCGC , CM000664.1:g.26705538_26705539insGTGTGTGTGTGTGAGTTGGCGC	GRCh37
NC_000002.10:g.26559042_26559043insGTGTGTGTGTGTGAGTTGGCGC	NCBI36
NG_009937.1:g.81033_81034insAACTCACACACACACACGCGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-74_1393-73insAACTCACACACACACACGCGCC MANE Select	ENSP00000272371.2:n.1393-74_1393-73insAACTCACACACACACACGCGCC
ENST00000272371.6:c.1393-74_1393-73insAACTCACACACACACACGCGCC	ENSP00000272371.2:n.1393-74_1393-73insAACTCACACACACACACGCGCC
ENST00000403946.7:c.1393-74_1393-73insAACTCACACACACACACGCGCC	ENSP00000385255.3:n.1393-74_1393-73insAACTCACACACACACACGCGCC
NM_001287489.1:c.1393-74_1393-73insAACTCACACACACACACGCGCC	NP_001274418.1:n.1393-74_1393-73insAACTCACACACACACACGCGCC
NM_194248.2:c.1393-74_1393-73insAACTCACACACACACACGCGCC	NP_919224.1:n.1393-74_1393-73insAACTCACACACACACACGCGCC
XM_005264644.2:c.1438-74_1438-73insAACTCACACACACACACGCGCC	XP_005264701.1:n.1438-74_1438-73insAACTCACACACACACACGCGCC
XM_011533185.1:c.1438-74_1438-73insAACTCACACACACACACGCGCC	XP_011531487.1:n.1438-74_1438-73insAACTCACACACACACACGCGCC
XM_017005338.1:c.1393-74_1393-73insAACTCACACACACACACGCGCC	XP_016860827.1:n.1393-74_1393-73insAACTCACACACACACACGCGCC
NM_001287489.2:c.1393-74_1393-73insAACTCACACACACACACGCGCC	NP_001274418.1:n.1393-74_1393-73insAACTCACACACACACACGCGCC
NM_194248.3:c.1393-74_1393-73insAACTCACACACACACACGCGCC MANE Select	NP_919224.1:n.1393-74_1393-73insAACTCACACACACACACGCGCC