Canonical Allele Identifier: CA1619384558

Gene: DXO

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969902G= , CM000668.2:g.31969902G=	GRCh38
NC_000006.11:g.31937679G= , CM000668.1:g.31937679G=	GRCh37
NC_000006.10:g.32045658G=	NCBI36
NG_032652.1:g.16099G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337523.10:c.1166C= MANE Select	ENSP00000337759.5:p.Pro389=
ENST00000337523.9:c.1166C=	ENSP00000337759.5:p.Pro389=
ENST00000375349.7:c.1166C=	ENSP00000364498.3:p.Pro389=
ENST00000375356.7:c.1166C=	ENSP00000364505.3:p.Pro389=
ENST00000473976.1:n.1938C=
ENST00000477826.5:n.2001C=
ENST00000478221.5:n.1047C=
ENST00000485557.5:n.1786C=
ENST00000491327.5:n.1303C=
ENST00000495340.5:c.499C=
ENST00000498357.1:n.1610C=
NM_005510.3:c.1166C=	NP_005501.2:p.Pro389=
XM_006715005.2:c.1166C=	XP_006715068.1:p.Pro389=
XM_006715007.2:c.614C=	XP_006715070.1:p.Pro205=
XR_926081.1:n.1639C=
XR_926082.1:n.1666C=
XM_006715005.3:c.1166C=	XP_006715068.1:p.Pro389=
XM_017010329.1:c.614C=	XP_016865818.1:p.Pro205=
XR_002956262.1:n.1398C=
XR_002956263.1:n.1564C=
XR_002956264.1:n.1464C=
XR_926082.2:n.1406C=
NM_005510.4:c.1166C= MANE Select	NP_005501.2:p.Pro389=
NM_001371205.1:c.614C=	NP_001358134.1:p.Pro205=
NM_001371206.1:c.614C=	NP_001358135.1:p.Pro205=