Canonical Allele Identifier: CA1239827753

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26480848_26480849delinsAG , CM000664.2:g.26480848_26480849delinsAG	GRCh38
NC_000002.11:g.26703716_26703717delinsAG , CM000664.1:g.26703716_26703717delinsAG	GRCh37
NC_000002.10:g.26557220_26557221delinsAG	NCBI36
NG_009937.1:g.82850_82851delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1740_1741delinsCT MANE Select	ENSP00000272371.2:p.Thr580=
ENST00000272371.6:c.1740_1741delinsCT	ENSP00000272371.2:p.Thr580=
ENST00000403946.7:c.1740_1741delinsCT	ENSP00000385255.3:p.Thr580=
NM_001287489.1:c.1740_1741delinsCT	NP_001274418.1:p.Thr580=
NM_194248.2:c.1740_1741delinsCT	NP_919224.1:p.Thr580=
XM_005264644.2:c.1785_1786delinsCT	XP_005264701.1:p.Thr595=
XM_011533185.1:c.1785_1786delinsCT	XP_011531487.1:p.Thr595=
XM_017005338.1:c.1740_1741delinsCT	XP_016860827.1:p.Thr580=
NM_001287489.2:c.1740_1741delinsCT	NP_001274418.1:p.Thr580=
NM_194248.3:c.1740_1741delinsCT MANE Select	NP_919224.1:p.Thr580=