Canonical Allele Identifier: CA2172870171

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42730760G= , CM000677.2:g.42730760G=	GRCh38
NC_000015.9:g.43022958G= , CM000677.1:g.43022958G=	GRCh37
NC_000015.8:g.40810250G=	NCBI36
NG_012491.1:g.11460C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.2012C= MANE Select	ENSP00000348564.3:p.Pro671=
ENST00000643434.1:c.*1190C=	ENSP00000494699.1:n.*1190C=
ENST00000356231.3:c.2012C=	ENSP00000348564.3:p.Pro671=
ENST00000562465.5:c.5C=	ENSP00000454246.1:p.Pro2=
NM_138477.2:c.2012C=	NP_612486.2:p.Pro671=
XM_005254176.3:c.2015C=	XP_005254233.1:p.Pro672=
XM_011521270.1:c.2039C=	XP_011519572.1:p.Pro680=
XM_011521271.1:c.2036C=	XP_011519573.1:p.Pro679=
XM_011521272.1:c.2039C=	XP_011519574.1:p.Pro680=
XM_011521273.1:c.2039C=	XP_011519575.1:p.Pro680=
XM_011521274.1:c.1004C=	XP_011519576.1:p.Pro335=
XM_011521275.1:c.1256C=	XP_011519577.1:p.Pro419=
XR_931757.1:n.2012C=
NM_138477.4:c.2012C= MANE Select	NP_612486.2:p.Pro671=
XM_005254176.5:c.2015C=	XP_005254233.1:p.Pro672=
XM_011521270.2:c.2039C=	XP_011519572.1:p.Pro680=
XM_011521271.2:c.2036C=	XP_011519573.1:p.Pro679=
XM_011521274.2:c.1004C=	XP_011519576.1:p.Pro335=
XR_001751104.1:n.2069C=
XR_001751105.1:n.2069C=
XR_931757.2:n.2032C=