Canonical Allele Identifier: CA2172869190

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42729073G= , CM000677.2:g.42729073G=	GRCh38
NC_000015.9:g.43021271G= , CM000677.1:g.43021271G=	GRCh37
NC_000015.8:g.40808563G=	NCBI36
NG_012491.1:g.13147C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000356231.4:c.2595C= MANE Select	ENSP00000348564.3:p.Thr865=
ENST00000643434.1:c.*1773C=	ENSP00000494699.1:n.*1773C=
ENST00000356231.3:c.2595C=	ENSP00000348564.3:p.Thr865=
ENST00000562465.5:c.588C=	ENSP00000454246.1:p.Thr196=
NM_138477.2:c.2595C=	NP_612486.2:p.Thr865=
XM_005254176.3:c.2598C=	XP_005254233.1:p.Thr866=
XM_011521270.1:c.2622C=	XP_011519572.1:p.Thr874=
XM_011521271.1:c.2619C=	XP_011519573.1:p.Thr873=
XM_011521272.1:c.2622C=	XP_011519574.1:p.Thr874=
XM_011521273.1:c.2622C=	XP_011519575.1:p.Thr874=
XM_011521274.1:c.1587C=	XP_011519576.1:p.Thr529=
XM_011521275.1:c.1839C=	XP_011519577.1:p.Thr613=
NM_138477.4:c.2595C= MANE Select	NP_612486.2:p.Thr865=
XM_005254176.5:c.2598C=	XP_005254233.1:p.Thr866=
XM_011521270.2:c.2622C=	XP_011519572.1:p.Thr874=
XM_011521271.2:c.2619C=	XP_011519573.1:p.Thr873=
XM_011521274.2:c.1587C=	XP_011519576.1:p.Thr529=
XR_001751104.1:n.2652C=
XR_001751105.1:n.2652C=