Canonical Allele Identifier: CA1619384522

Gene: DXO SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969839T= , CM000668.2:g.31969839T=	GRCh38
NC_000006.11:g.31937616T= , CM000668.1:g.31937616T=	GRCh37
NC_000006.10:g.32045595T=	NCBI36
NG_032652.1:g.16036T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337523.10:c.*38A= (DXO) MANE Select	ENSP00000337759.5:n.*38A=
ENST00000337523.9:c.*38A= (DXO)	ENSP00000337759.5:n.*38A=
ENST00000375349.7:c.*38A= (DXO)	ENSP00000364498.3:n.*38A=
ENST00000473976.1:n.2001A= (DXO)
ENST00000477826.5:n.2064A= (DXO)
ENST00000478221.5:n.1110A= (DXO)
ENST00000485557.5:n.1849A= (DXO)
ENST00000491327.5:n.1366A= (DXO)
ENST00000495340.5:c.562A= (DXO)
NM_005510.3:c.*38A= (DXO)	NP_005501.2:n.*38A=
XM_006715005.2:c.*38A= (DXO)	XP_006715068.1:n.*38A=
XM_006715007.2:c.*38A= (DXO)	XP_006715070.1:n.*38A=
XR_926081.1:n.1702A= (DXO)
XR_926082.1:n.1729A= (DXO)
XM_006715005.3:c.*38A= (DXO)	XP_006715068.1:n.*38A=
XM_017010329.1:c.*38A= (DXO)	XP_016865818.1:n.*38A=
XR_002956262.1:n.1461A= (DXO)
XR_002956263.1:n.1627A= (DXO)
XR_002956264.1:n.1527A= (DXO)
XR_926082.2:n.1469A= (DXO)
XR_926301.3:n.3881T= (SKIC2)
NM_005510.4:c.*38A= (DXO) MANE Select	NP_005501.2:n.*38A=
NM_001371205.1:c.*38A= (DXO)	NP_001358134.1:n.*38A=
NM_001371206.1:c.*38A= (DXO)	NP_001358135.1:n.*38A=