Canonical Allele Identifier: CA1619384541

Gene: DXO

Linked Data

• dbSNP Id: rs1582193609

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969871G>C , CM000668.2:g.31969871G>C	GRCh38
NC_000006.11:g.31937648G>C , CM000668.1:g.31937648G>C	GRCh37
NC_000006.10:g.32045627G>C	NCBI36
NG_032652.1:g.16068G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337523.10:c.*6C>G MANE Select	ENSP00000337759.5:n.*6C>G
ENST00000337523.9:c.*6C>G	ENSP00000337759.5:n.*6C>G
ENST00000375349.7:c.*6C>G	ENSP00000364498.3:n.*6C>G
ENST00000375356.7:c.*6C>G	ENSP00000364505.3:n.*6C>G
ENST00000473976.1:n.1969C>G
ENST00000477826.5:n.2032C>G
ENST00000478221.5:n.1078C>G
ENST00000485557.5:n.1817C>G
ENST00000491327.5:n.1334C>G
ENST00000495340.5:c.530C>G
NM_005510.3:c.*6C>G	NP_005501.2:n.*6C>G
XM_006715005.2:c.*6C>G	XP_006715068.1:n.*6C>G
XM_006715007.2:c.*6C>G	XP_006715070.1:n.*6C>G
XR_926081.1:n.1670C>G
XR_926082.1:n.1697C>G
XM_006715005.3:c.*6C>G	XP_006715068.1:n.*6C>G
XM_017010329.1:c.*6C>G	XP_016865818.1:n.*6C>G
XR_002956262.1:n.1429C>G
XR_002956263.1:n.1595C>G
XR_002956264.1:n.1495C>G
XR_926082.2:n.1437C>G
NM_005510.4:c.*6C>G MANE Select	NP_005501.2:n.*6C>G
NM_001371205.1:c.*6C>G	NP_001358134.1:n.*6C>G
NM_001371206.1:c.*6C>G	NP_001358135.1:n.*6C>G