Canonical Allele Identifier: CA363492952
Gene: DXO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31969896T>C , CM000668.2:g.31969896T>C GRCh38
NC_000006.11:g.31937673T>C , CM000668.1:g.31937673T>C GRCh37
NC_000006.10:g.32045652T>C NCBI36
NG_032652.1:g.16093T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000337523.10:c.1172A>G MANE Select ENSP00000337759.5:p.Lys391Arg
ENST00000337523.9:c.1172A>G ENSP00000337759.5:p.Lys391Arg
ENST00000375349.7:c.1172A>G ENSP00000364498.3:p.Lys391Arg
ENST00000375356.7:c.1172A>G ENSP00000364505.3:p.Lys391Arg
ENST00000473976.1:n.1944A>G
ENST00000477826.5:n.2007A>G
ENST00000478221.5:n.1053A>G
ENST00000485557.5:n.1792A>G
ENST00000491327.5:n.1309A>G
ENST00000495340.5:c.505A>G
ENST00000498357.1:n.1616A>G
NM_005510.3:c.1172A>G NP_005501.2:p.Lys391Arg
XM_006715005.2:c.1172A>G XP_006715068.1:p.Lys391Arg
XM_006715007.2:c.620A>G XP_006715070.1:p.Lys207Arg
XR_926081.1:n.1645A>G
XR_926082.1:n.1672A>G
XM_006715005.3:c.1172A>G XP_006715068.1:p.Lys391Arg
XM_017010329.1:c.620A>G XP_016865818.1:p.Lys207Arg
XR_002956262.1:n.1404A>G
XR_002956263.1:n.1570A>G
XR_002956264.1:n.1470A>G
XR_926082.2:n.1412A>G
NM_005510.4:c.1172A>G MANE Select NP_005501.2:p.Lys391Arg
NM_001371205.1:c.620A>G NP_001358134.1:p.Lys207Arg
NM_001371206.1:c.620A>G NP_001358135.1:p.Lys207Arg