Canonical Allele Identifier: CA2576699734

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482678_26482679insATGT , CM000664.2:g.26482678_26482679insATGT	GRCh38
NC_000002.11:g.26705546_26705547insATGT , CM000664.1:g.26705546_26705547insATGT	GRCh37
NC_000002.10:g.26559050_26559051insATGT	NCBI36
NG_009937.1:g.81020_81021insACAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-87_1393-86insACAT MANE Select	ENSP00000272371.2:n.1393-87_1393-86insACAT
ENST00000272371.6:c.1393-87_1393-86insACAT	ENSP00000272371.2:n.1393-87_1393-86insACAT
ENST00000403946.7:c.1393-87_1393-86insACAT	ENSP00000385255.3:n.1393-87_1393-86insACAT
NM_001287489.1:c.1393-87_1393-86insACAT	NP_001274418.1:n.1393-87_1393-86insACAT
NM_194248.2:c.1393-87_1393-86insACAT	NP_919224.1:n.1393-87_1393-86insACAT
XM_005264644.2:c.1438-87_1438-86insACAT	XP_005264701.1:n.1438-87_1438-86insACAT
XM_011533185.1:c.1438-87_1438-86insACAT	XP_011531487.1:n.1438-87_1438-86insACAT
XM_017005338.1:c.1393-87_1393-86insACAT	XP_016860827.1:n.1393-87_1393-86insACAT
NM_001287489.2:c.1393-87_1393-86insACAT	NP_001274418.1:n.1393-87_1393-86insACAT
NM_194248.3:c.1393-87_1393-86insACAT MANE Select	NP_919224.1:n.1393-87_1393-86insACAT