Canonical Allele Identifier: CA2172870100

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42730640T= , CM000677.2:g.42730640T=	GRCh38
NC_000015.9:g.43022838T= , CM000677.1:g.43022838T=	GRCh37
NC_000015.8:g.40810130T=	NCBI36
NG_012491.1:g.11580A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.2132A= MANE Select	ENSP00000348564.3:p.Glu711=
ENST00000643434.1:c.*1310A=	ENSP00000494699.1:n.*1310A=
ENST00000356231.3:c.2132A=	ENSP00000348564.3:p.Glu711=
ENST00000562465.5:c.125A=	ENSP00000454246.1:p.Glu42=
NM_138477.2:c.2132A=	NP_612486.2:p.Glu711=
XM_005254176.3:c.2135A=	XP_005254233.1:p.Glu712=
XM_011521270.1:c.2159A=	XP_011519572.1:p.Glu720=
XM_011521271.1:c.2156A=	XP_011519573.1:p.Glu719=
XM_011521272.1:c.2159A=	XP_011519574.1:p.Glu720=
XM_011521273.1:c.2159A=	XP_011519575.1:p.Glu720=
XM_011521274.1:c.1124A=	XP_011519576.1:p.Glu375=
XM_011521275.1:c.1376A=	XP_011519577.1:p.Glu459=
XR_931757.1:n.2132A=
NM_138477.4:c.2132A= MANE Select	NP_612486.2:p.Glu711=
XM_005254176.5:c.2135A=	XP_005254233.1:p.Glu712=
XM_011521270.2:c.2159A=	XP_011519572.1:p.Glu720=
XM_011521271.2:c.2156A=	XP_011519573.1:p.Glu719=
XM_011521274.2:c.1124A=	XP_011519576.1:p.Glu375=
XR_001751104.1:n.2189A=
XR_001751105.1:n.2189A=
XR_931757.2:n.2152A=