Canonical Allele Identifier: CA645559539

Gene: DXO

Linked Data

• COSMIC: COSM143528

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969898_31969899delinsAC , CM000668.2:g.31969898_31969899delinsAC	GRCh38
NC_000006.11:g.31937675_31937676delinsAC , CM000668.1:g.31937675_31937676delinsAC	GRCh37
NC_000006.10:g.32045654_32045655delinsAC	NCBI36
NG_032652.1:g.16095_16096delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337523.10:c.1169_1170delinsGT MANE Select	ENSP00000337759.5:p.Pro390Arg
ENST00000337523.9:c.1169_1170delinsGT	ENSP00000337759.5:p.Pro390Arg
ENST00000375349.7:c.1169_1170delinsGT	ENSP00000364498.3:p.Pro390Arg
ENST00000375356.7:c.1169_1170delinsGT	ENSP00000364505.3:p.Pro390Arg
ENST00000473976.1:n.1941_1942delinsGT
ENST00000477826.5:n.2004_2005delinsGT
ENST00000478221.5:n.1050_1051delinsGT
ENST00000485557.5:n.1789_1790delinsGT
ENST00000491327.5:n.1306_1307delinsGT
ENST00000495340.5:c.502_503delinsGT
ENST00000498357.1:n.1613_1614delinsGT
NM_005510.3:c.1169_1170delinsGT	NP_005501.2:p.Pro390Arg
XM_006715005.2:c.1169_1170delinsGT	XP_006715068.1:p.Pro390Arg
XM_006715007.2:c.617_618delinsGT	XP_006715070.1:p.Pro206Arg
XR_926081.1:n.1642_1643delinsGT
XR_926082.1:n.1669_1670delinsGT
XM_006715005.3:c.1169_1170delinsGT	XP_006715068.1:p.Pro390Arg
XM_017010329.1:c.617_618delinsGT	XP_016865818.1:p.Pro206Arg
XR_002956262.1:n.1401_1402delinsGT
XR_002956263.1:n.1567_1568delinsGT
XR_002956264.1:n.1467_1468delinsGT
XR_926082.2:n.1409_1410delinsGT
NM_005510.4:c.1169_1170delinsGT MANE Select	NP_005501.2:p.Pro390Arg
NM_001371205.1:c.617_618delinsGT	NP_001358134.1:p.Pro206Arg
NM_001371206.1:c.617_618delinsGT	NP_001358135.1:p.Pro206Arg