Canonical Allele Identifier: CA2678079132

Gene: DXO

Linked Data

• gnomAD v4: 6-31969866-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969866C>T , CM000668.2:g.31969866C>T	GRCh38
NC_000006.11:g.31937643C>T , CM000668.1:g.31937643C>T	GRCh37
NC_000006.10:g.32045622C>T	NCBI36
NG_032652.1:g.16063C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337523.10:c.*11G>A MANE Select	ENSP00000337759.5:n.*11G>A
ENST00000337523.9:c.*11G>A	ENSP00000337759.5:n.*11G>A
ENST00000375349.7:c.*11G>A	ENSP00000364498.3:n.*11G>A
ENST00000375356.7:c.*11G>A	ENSP00000364505.3:n.*11G>A
ENST00000473976.1:n.1974G>A
ENST00000477826.5:n.2037G>A
ENST00000478221.5:n.1083G>A
ENST00000485557.5:n.1822G>A
ENST00000491327.5:n.1339G>A
ENST00000495340.5:c.535G>A
NM_005510.3:c.*11G>A	NP_005501.2:n.*11G>A
XM_006715005.2:c.*11G>A	XP_006715068.1:n.*11G>A
XM_006715007.2:c.*11G>A	XP_006715070.1:n.*11G>A
XR_926081.1:n.1675G>A
XR_926082.1:n.1702G>A
XM_006715005.3:c.*11G>A	XP_006715068.1:n.*11G>A
XM_017010329.1:c.*11G>A	XP_016865818.1:n.*11G>A
XR_002956262.1:n.1434G>A
XR_002956263.1:n.1600G>A
XR_002956264.1:n.1500G>A
XR_926082.2:n.1442G>A
NM_005510.4:c.*11G>A MANE Select	NP_005501.2:n.*11G>A
NM_001371205.1:c.*11G>A	NP_001358134.1:n.*11G>A
NM_001371206.1:c.*11G>A	NP_001358135.1:n.*11G>A