Canonical Allele Identifier: CA363492935

Gene: DXO

Linked Data

• MyVariant Identifiers: chr6:g.31937670G>T (hg19) ; chr6:g.31969893G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969893G>T , CM000668.2:g.31969893G>T	GRCh38
NC_000006.11:g.31937670G>T , CM000668.1:g.31937670G>T	GRCh37
NC_000006.10:g.32045649G>T	NCBI36
NG_032652.1:g.16090G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337523.10:c.1175C>A MANE Select	ENSP00000337759.5:p.Thr392Asn
ENST00000337523.9:c.1175C>A	ENSP00000337759.5:p.Thr392Asn
ENST00000375349.7:c.1175C>A	ENSP00000364498.3:p.Thr392Asn
ENST00000375356.7:c.1175C>A	ENSP00000364505.3:p.Thr392Asn
ENST00000473976.1:n.1947C>A
ENST00000477826.5:n.2010C>A
ENST00000478221.5:n.1056C>A
ENST00000485557.5:n.1795C>A
ENST00000491327.5:n.1312C>A
ENST00000495340.5:c.508C>A
ENST00000498357.1:n.1619C>A
NM_005510.3:c.1175C>A	NP_005501.2:p.Thr392Asn
XM_006715005.2:c.1175C>A	XP_006715068.1:p.Thr392Asn
XM_006715007.2:c.623C>A	XP_006715070.1:p.Thr208Asn
XR_926081.1:n.1648C>A
XR_926082.1:n.1675C>A
XM_006715005.3:c.1175C>A	XP_006715068.1:p.Thr392Asn
XM_017010329.1:c.623C>A	XP_016865818.1:p.Thr208Asn
XR_002956262.1:n.1407C>A
XR_002956263.1:n.1573C>A
XR_002956264.1:n.1473C>A
XR_926082.2:n.1415C>A
NM_005510.4:c.1175C>A MANE Select	NP_005501.2:p.Thr392Asn
NM_001371205.1:c.623C>A	NP_001358134.1:p.Thr208Asn
NM_001371206.1:c.623C>A	NP_001358135.1:p.Thr208Asn