Canonical Allele Identifier: CA1239829215

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482627_26482629delinsATG , CM000664.2:g.26482627_26482629delinsATG	GRCh38
NC_000002.11:g.26705495_26705497delinsATG , CM000664.1:g.26705495_26705497delinsATG	GRCh37
NC_000002.10:g.26558999_26559001delinsATG	NCBI36
NG_009937.1:g.81070_81072delinsCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-37_1393-35delinsCAT MANE Select	ENSP00000272371.2:n.1393-37_1393-35delinsCAT
ENST00000272371.6:c.1393-37_1393-35delinsCAT	ENSP00000272371.2:n.1393-37_1393-35delinsCAT
ENST00000403946.7:c.1393-37_1393-35delinsCAT	ENSP00000385255.3:n.1393-37_1393-35delinsCAT
NM_001287489.1:c.1393-37_1393-35delinsCAT	NP_001274418.1:n.1393-37_1393-35delinsCAT
NM_194248.2:c.1393-37_1393-35delinsCAT	NP_919224.1:n.1393-37_1393-35delinsCAT
XM_005264644.2:c.1438-37_1438-35delinsCAT	XP_005264701.1:n.1438-37_1438-35delinsCAT
XM_011533185.1:c.1438-37_1438-35delinsCAT	XP_011531487.1:n.1438-37_1438-35delinsCAT
XM_017005338.1:c.1393-37_1393-35delinsCAT	XP_016860827.1:n.1393-37_1393-35delinsCAT
NM_001287489.2:c.1393-37_1393-35delinsCAT	NP_001274418.1:n.1393-37_1393-35delinsCAT
NM_194248.3:c.1393-37_1393-35delinsCAT MANE Select	NP_919224.1:n.1393-37_1393-35delinsCAT