Canonical Allele Identifier: CA1619384554

Gene: DXO

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969897_31969898delinsTG , CM000668.2:g.31969897_31969898delinsTG	GRCh38
NC_000006.11:g.31937674_31937675delinsTG , CM000668.1:g.31937674_31937675delinsTG	GRCh37
NC_000006.10:g.32045653_32045654delinsTG	NCBI36
NG_032652.1:g.16094_16095delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337523.10:c.1170_1171delinsCA MANE Select	ENSP00000337759.5:p.Pro390=
ENST00000337523.9:c.1170_1171delinsCA	ENSP00000337759.5:p.Pro390=
ENST00000375349.7:c.1170_1171delinsCA	ENSP00000364498.3:p.Pro390=
ENST00000375356.7:c.1170_1171delinsCA	ENSP00000364505.3:p.Pro390=
ENST00000473976.1:n.1942_1943delinsCA
ENST00000477826.5:n.2005_2006delinsCA
ENST00000478221.5:n.1051_1052delinsCA
ENST00000485557.5:n.1790_1791delinsCA
ENST00000491327.5:n.1307_1308delinsCA
ENST00000495340.5:c.503_504delinsCA
ENST00000498357.1:n.1614_1615delinsCA
NM_005510.3:c.1170_1171delinsCA	NP_005501.2:p.Pro390=
XM_006715005.2:c.1170_1171delinsCA	XP_006715068.1:p.Pro390=
XM_006715007.2:c.618_619delinsCA	XP_006715070.1:p.Pro206=
XR_926081.1:n.1643_1644delinsCA
XR_926082.1:n.1670_1671delinsCA
XM_006715005.3:c.1170_1171delinsCA	XP_006715068.1:p.Pro390=
XM_017010329.1:c.618_619delinsCA	XP_016865818.1:p.Pro206=
XR_002956262.1:n.1402_1403delinsCA
XR_002956263.1:n.1568_1569delinsCA
XR_002956264.1:n.1468_1469delinsCA
XR_926082.2:n.1410_1411delinsCA
NM_005510.4:c.1170_1171delinsCA MANE Select	NP_005501.2:p.Pro390=
NM_001371205.1:c.618_619delinsCA	NP_001358134.1:p.Pro206=
NM_001371206.1:c.618_619delinsCA	NP_001358135.1:p.Pro206=