Canonical Allele Identifier: CA2678079113

Gene: DXO

Linked Data

• gnomAD v4: 6-31969858-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969858G>A , CM000668.2:g.31969858G>A	GRCh38
NC_000006.11:g.31937635G>A , CM000668.1:g.31937635G>A	GRCh37
NC_000006.10:g.32045614G>A	NCBI36
NG_032652.1:g.16055G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337523.10:c.*19C>T MANE Select	ENSP00000337759.5:n.*19C>T
ENST00000337523.9:c.*19C>T	ENSP00000337759.5:n.*19C>T
ENST00000375349.7:c.*19C>T	ENSP00000364498.3:n.*19C>T
ENST00000375356.7:c.*19C>T	ENSP00000364505.3:n.*19C>T
ENST00000473976.1:n.1982C>T
ENST00000477826.5:n.2045C>T
ENST00000478221.5:n.1091C>T
ENST00000485557.5:n.1830C>T
ENST00000491327.5:n.1347C>T
ENST00000495340.5:c.543C>T
NM_005510.3:c.*19C>T	NP_005501.2:n.*19C>T
XM_006715005.2:c.*19C>T	XP_006715068.1:n.*19C>T
XM_006715007.2:c.*19C>T	XP_006715070.1:n.*19C>T
XR_926081.1:n.1683C>T
XR_926082.1:n.1710C>T
XM_006715005.3:c.*19C>T	XP_006715068.1:n.*19C>T
XM_017010329.1:c.*19C>T	XP_016865818.1:n.*19C>T
XR_002956262.1:n.1442C>T
XR_002956263.1:n.1608C>T
XR_002956264.1:n.1508C>T
XR_926082.2:n.1450C>T
NM_005510.4:c.*19C>T MANE Select	NP_005501.2:n.*19C>T
NM_001371205.1:c.*19C>T	NP_001358134.1:n.*19C>T
NM_001371206.1:c.*19C>T	NP_001358135.1:n.*19C>T