Canonical Allele Identifier: CA2172870094

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42730632G= , CM000677.2:g.42730632G=	GRCh38
NC_000015.9:g.43022830G= , CM000677.1:g.43022830G=	GRCh37
NC_000015.8:g.40810122G=	NCBI36
NG_012491.1:g.11588C=

Transcript Alleles

HGVS	Amino-acid Change
NM_138477.4:c.2140C= MANE Select	NP_612486.2:p.Arg714=
ENST00000356231.4:c.2140C= MANE Select	ENSP00000348564.3:p.Arg714=
NM_138477.2:c.2140C=	NP_612486.2:p.Arg714=
ENST00000356231.3:c.2140C=	ENSP00000348564.3:p.Arg714=
ENST00000562465.5:c.133C=	ENSP00000454246.1:p.Arg45=
ENST00000643434.1:c.*1318C=	ENSP00000494699.1:n.*1318C=
XM_005254176.3:c.2143C=	XP_005254233.1:p.Arg715=
XM_005254176.5:c.2143C=	XP_005254233.1:p.Arg715=
XM_011521270.1:c.2167C=	XP_011519572.1:p.Arg723=
XM_011521270.2:c.2167C=	XP_011519572.1:p.Arg723=
XM_011521271.1:c.2164C=	XP_011519573.1:p.Arg722=
XM_011521271.2:c.2164C=	XP_011519573.1:p.Arg722=
XM_011521272.1:c.2167C=	XP_011519574.1:p.Arg723=
XM_011521273.1:c.2167C=	XP_011519575.1:p.Arg723=
XM_011521274.1:c.1132C=	XP_011519576.1:p.Arg378=
XM_011521274.2:c.1132C=	XP_011519576.1:p.Arg378=
XM_011521275.1:c.1384C=	XP_011519577.1:p.Arg462=
XR_001751104.1:n.2197C=
XR_001751105.1:n.2197C=
XR_931757.1:n.2140C=
XR_931757.2:n.2160C=