Canonical Allele Identifier: CA1619384545

Gene: DXO

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969878T= , CM000668.2:g.31969878T=	GRCh38
NC_000006.11:g.31937655T= , CM000668.1:g.31937655T=	GRCh37
NC_000006.10:g.32045634T=	NCBI36
NG_032652.1:g.16075T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337523.10:c.1190A= MANE Select	ENSP00000337759.5:p.Ter397=
ENST00000337523.9:c.1190A=	ENSP00000337759.5:p.Ter397=
ENST00000375349.7:c.1190A=	ENSP00000364498.3:p.Ter397=
ENST00000375356.7:c.1190A=	ENSP00000364505.3:p.Ter397=
ENST00000473976.1:n.1962A=
ENST00000477826.5:n.2025A=
ENST00000478221.5:n.1071A=
ENST00000485557.5:n.1810A=
ENST00000491327.5:n.1327A=
ENST00000495340.5:c.523A=
NM_005510.3:c.1190A=	NP_005501.2:p.Ter397=
XM_006715005.2:c.1190A=	XP_006715068.1:p.Ter397=
XM_006715007.2:c.638A=	XP_006715070.1:p.Ter213=
XR_926081.1:n.1663A=
XR_926082.1:n.1690A=
XM_006715005.3:c.1190A=	XP_006715068.1:p.Ter397=
XM_017010329.1:c.638A=	XP_016865818.1:p.Ter213=
XR_002956262.1:n.1422A=
XR_002956263.1:n.1588A=
XR_002956264.1:n.1488A=
XR_926082.2:n.1430A=
NM_005510.4:c.1190A= MANE Select	NP_005501.2:p.Ter397=
NM_001371205.1:c.638A=	NP_001358134.1:p.Ter213=
NM_001371206.1:c.638A=	NP_001358135.1:p.Ter213=