Canonical Allele Identifier: CA2576699743

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26483392_26483410del , CM000664.2:g.26483392_26483410del	GRCh38
NC_000002.11:g.26706260_26706278del , CM000664.1:g.26706260_26706278del	GRCh37
NC_000002.10:g.26559764_26559782del	NCBI36
NG_009937.1:g.80293_80311del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1392+56_1392+74del MANE Select	ENSP00000272371.2:n.1392+56_1392+74del
ENST00000272371.6:c.1392+56_1392+74del	ENSP00000272371.2:n.1392+56_1392+74del
ENST00000403946.7:c.1392+56_1392+74del	ENSP00000385255.3:n.1392+56_1392+74del
NM_001287489.1:c.1392+56_1392+74del	NP_001274418.1:n.1392+56_1392+74del
NM_194248.2:c.1392+56_1392+74del	NP_919224.1:n.1392+56_1392+74del
XM_005264644.2:c.1437+56_1437+74del	XP_005264701.1:n.1437+56_1437+74del
XM_011533185.1:c.1437+56_1437+74del	XP_011531487.1:n.1437+56_1437+74del
XM_017005338.1:c.1392+56_1392+74del	XP_016860827.1:n.1392+56_1392+74del
NM_001287489.2:c.1392+56_1392+74del	NP_001274418.1:n.1392+56_1392+74del
NM_194248.3:c.1392+56_1392+74del MANE Select	NP_919224.1:n.1392+56_1392+74del