Canonical Allele Identifier: CA2678079111

Gene: DXO

Linked Data

• gnomAD v4: 6-31969853-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969853T>C , CM000668.2:g.31969853T>C	GRCh38
NC_000006.11:g.31937630T>C , CM000668.1:g.31937630T>C	GRCh37
NC_000006.10:g.32045609T>C	NCBI36
NG_032652.1:g.16050T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337523.10:c.*24A>G MANE Select	ENSP00000337759.5:n.*24A>G
ENST00000337523.9:c.*24A>G	ENSP00000337759.5:n.*24A>G
ENST00000375349.7:c.*24A>G	ENSP00000364498.3:n.*24A>G
ENST00000375356.7:c.*24A>G	ENSP00000364505.3:n.*24A>G
ENST00000473976.1:n.1987A>G
ENST00000477826.5:n.2050A>G
ENST00000478221.5:n.1096A>G
ENST00000485557.5:n.1835A>G
ENST00000491327.5:n.1352A>G
ENST00000495340.5:c.548A>G
NM_005510.3:c.*24A>G	NP_005501.2:n.*24A>G
XM_006715005.2:c.*24A>G	XP_006715068.1:n.*24A>G
XM_006715007.2:c.*24A>G	XP_006715070.1:n.*24A>G
XR_926081.1:n.1688A>G
XR_926082.1:n.1715A>G
XM_006715005.3:c.*24A>G	XP_006715068.1:n.*24A>G
XM_017010329.1:c.*24A>G	XP_016865818.1:n.*24A>G
XR_002956262.1:n.1447A>G
XR_002956263.1:n.1613A>G
XR_002956264.1:n.1513A>G
XR_926082.2:n.1455A>G
NM_005510.4:c.*24A>G MANE Select	NP_005501.2:n.*24A>G
NM_001371205.1:c.*24A>G	NP_001358134.1:n.*24A>G
NM_001371206.1:c.*24A>G	NP_001358135.1:n.*24A>G