Canonical Allele Identifier: CA1619384556

Gene: DXO

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969899G= , CM000668.2:g.31969899G=	GRCh38
NC_000006.11:g.31937676G= , CM000668.1:g.31937676G=	GRCh37
NC_000006.10:g.32045655G=	NCBI36
NG_032652.1:g.16096G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337523.10:c.1169C= MANE Select	ENSP00000337759.5:p.Pro390=
ENST00000337523.9:c.1169C=	ENSP00000337759.5:p.Pro390=
ENST00000375349.7:c.1169C=	ENSP00000364498.3:p.Pro390=
ENST00000375356.7:c.1169C=	ENSP00000364505.3:p.Pro390=
ENST00000473976.1:n.1941C=
ENST00000477826.5:n.2004C=
ENST00000478221.5:n.1050C=
ENST00000485557.5:n.1789C=
ENST00000491327.5:n.1306C=
ENST00000495340.5:c.502C=
ENST00000498357.1:n.1613C=
NM_005510.3:c.1169C=	NP_005501.2:p.Pro390=
XM_006715005.2:c.1169C=	XP_006715068.1:p.Pro390=
XM_006715007.2:c.617C=	XP_006715070.1:p.Pro206=
XR_926081.1:n.1642C=
XR_926082.1:n.1669C=
XM_006715005.3:c.1169C=	XP_006715068.1:p.Pro390=
XM_017010329.1:c.617C=	XP_016865818.1:p.Pro206=
XR_002956262.1:n.1401C=
XR_002956263.1:n.1567C=
XR_002956264.1:n.1467C=
XR_926082.2:n.1409C=
NM_005510.4:c.1169C= MANE Select	NP_005501.2:p.Pro390=
NM_001371205.1:c.617C=	NP_001358134.1:p.Pro206=
NM_001371206.1:c.617C=	NP_001358135.1:p.Pro206=