Canonical Allele Identifier: CA363492941

Gene: DXO

Linked Data

• MyVariant Identifiers: chr6:g.31937671T>A (hg19) ; chr6:g.31969894T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969894T>A , CM000668.2:g.31969894T>A	GRCh38
NC_000006.11:g.31937671T>A , CM000668.1:g.31937671T>A	GRCh37
NC_000006.10:g.32045650T>A	NCBI36
NG_032652.1:g.16091T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337523.10:c.1174A>T MANE Select	ENSP00000337759.5:p.Thr392Ser
ENST00000337523.9:c.1174A>T	ENSP00000337759.5:p.Thr392Ser
ENST00000375349.7:c.1174A>T	ENSP00000364498.3:p.Thr392Ser
ENST00000375356.7:c.1174A>T	ENSP00000364505.3:p.Thr392Ser
ENST00000473976.1:n.1946A>T
ENST00000477826.5:n.2009A>T
ENST00000478221.5:n.1055A>T
ENST00000485557.5:n.1794A>T
ENST00000491327.5:n.1311A>T
ENST00000495340.5:c.507A>T
ENST00000498357.1:n.1618A>T
NM_005510.3:c.1174A>T	NP_005501.2:p.Thr392Ser
XM_006715005.2:c.1174A>T	XP_006715068.1:p.Thr392Ser
XM_006715007.2:c.622A>T	XP_006715070.1:p.Thr208Ser
XR_926081.1:n.1647A>T
XR_926082.1:n.1674A>T
XM_006715005.3:c.1174A>T	XP_006715068.1:p.Thr392Ser
XM_017010329.1:c.622A>T	XP_016865818.1:p.Thr208Ser
XR_002956262.1:n.1406A>T
XR_002956263.1:n.1572A>T
XR_002956264.1:n.1472A>T
XR_926082.2:n.1414A>T
NM_005510.4:c.1174A>T MANE Select	NP_005501.2:p.Thr392Ser
NM_001371205.1:c.622A>T	NP_001358134.1:p.Thr208Ser
NM_001371206.1:c.622A>T	NP_001358135.1:p.Thr208Ser