Canonical Allele Identifier: CA449814223

Gene: DXO

Linked Data

• MyVariant Identifiers: chr6:g.31937666G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969889G>C , CM000668.2:g.31969889G>C	GRCh38
NC_000006.11:g.31937666G>C , CM000668.1:g.31937666G>C	GRCh37
NC_000006.10:g.32045645G>C	NCBI36
NG_032652.1:g.16086G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337523.10:c.1179C>G MANE Select	ENSP00000337759.5:p.Pro393=
ENST00000337523.9:c.1179C>G	ENSP00000337759.5:p.Pro393=
ENST00000375349.7:c.1179C>G	ENSP00000364498.3:p.Pro393=
ENST00000375356.7:c.1179C>G	ENSP00000364505.3:p.Pro393=
ENST00000473976.1:n.1951C>G
ENST00000477826.5:n.2014C>G
ENST00000478221.5:n.1060C>G
ENST00000485557.5:n.1799C>G
ENST00000491327.5:n.1316C>G
ENST00000495340.5:c.512C>G
ENST00000498357.1:n.1623C>G
NM_005510.3:c.1179C>G	NP_005501.2:p.Pro393=
XM_006715005.2:c.1179C>G	XP_006715068.1:p.Pro393=
XM_006715007.2:c.627C>G	XP_006715070.1:p.Pro209=
XR_926081.1:n.1652C>G
XR_926082.1:n.1679C>G
XM_006715005.3:c.1179C>G	XP_006715068.1:p.Pro393=
XM_017010329.1:c.627C>G	XP_016865818.1:p.Pro209=
XR_002956262.1:n.1411C>G
XR_002956263.1:n.1577C>G
XR_002956264.1:n.1477C>G
XR_926082.2:n.1419C>G
NM_005510.4:c.1179C>G MANE Select	NP_005501.2:p.Pro393=
NM_001371205.1:c.627C>G	NP_001358134.1:p.Pro209=
NM_001371206.1:c.627C>G	NP_001358135.1:p.Pro209=