Canonical Allele Identifier: CA1619384538

Gene: DXO

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969862C= , CM000668.2:g.31969862C=	GRCh38
NC_000006.11:g.31937639C= , CM000668.1:g.31937639C=	GRCh37
NC_000006.10:g.32045618C=	NCBI36
NG_032652.1:g.16059C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337523.10:c.*15G= MANE Select	ENSP00000337759.5:n.*15G=
ENST00000337523.9:c.*15G=	ENSP00000337759.5:n.*15G=
ENST00000375349.7:c.*15G=	ENSP00000364498.3:n.*15G=
ENST00000375356.7:c.*15G=	ENSP00000364505.3:n.*15G=
ENST00000473976.1:n.1978G=
ENST00000477826.5:n.2041G=
ENST00000478221.5:n.1087G=
ENST00000485557.5:n.1826G=
ENST00000491327.5:n.1343G=
ENST00000495340.5:c.539G=
NM_005510.3:c.*15G=	NP_005501.2:n.*15G=
XM_006715005.2:c.*15G=	XP_006715068.1:n.*15G=
XM_006715007.2:c.*15G=	XP_006715070.1:n.*15G=
XR_926081.1:n.1679G=
XR_926082.1:n.1706G=
XM_006715005.3:c.*15G=	XP_006715068.1:n.*15G=
XM_017010329.1:c.*15G=	XP_016865818.1:n.*15G=
XR_002956262.1:n.1438G=
XR_002956263.1:n.1604G=
XR_002956264.1:n.1504G=
XR_926082.2:n.1446G=
NM_005510.4:c.*15G= MANE Select	NP_005501.2:n.*15G=
NM_001371205.1:c.*15G=	NP_001358134.1:n.*15G=
NM_001371206.1:c.*15G=	NP_001358135.1:n.*15G=