Canonical Allele Identifier: CA2172869193

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42729077C= , CM000677.2:g.42729077C=	GRCh38
NC_000015.9:g.43021275C= , CM000677.1:g.43021275C=	GRCh37
NC_000015.8:g.40808567C=	NCBI36
NG_012491.1:g.13143G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000356231.4:c.2591G= MANE Select	ENSP00000348564.3:p.Arg864=
ENST00000643434.1:c.*1769G=	ENSP00000494699.1:n.*1769G=
ENST00000356231.3:c.2591G=	ENSP00000348564.3:p.Arg864=
ENST00000562465.5:c.584G=	ENSP00000454246.1:p.Arg195=
NM_138477.2:c.2591G=	NP_612486.2:p.Arg864=
XM_005254176.3:c.2594G=	XP_005254233.1:p.Arg865=
XM_011521270.1:c.2618G=	XP_011519572.1:p.Arg873=
XM_011521271.1:c.2615G=	XP_011519573.1:p.Arg872=
XM_011521272.1:c.2618G=	XP_011519574.1:p.Arg873=
XM_011521273.1:c.2618G=	XP_011519575.1:p.Arg873=
XM_011521274.1:c.1583G=	XP_011519576.1:p.Arg528=
XM_011521275.1:c.1835G=	XP_011519577.1:p.Arg612=
NM_138477.4:c.2591G= MANE Select	NP_612486.2:p.Arg864=
XM_005254176.5:c.2594G=	XP_005254233.1:p.Arg865=
XM_011521270.2:c.2618G=	XP_011519572.1:p.Arg873=
XM_011521271.2:c.2615G=	XP_011519573.1:p.Arg872=
XM_011521274.2:c.1583G=	XP_011519576.1:p.Arg528=
XR_001751104.1:n.2648G=
XR_001751105.1:n.2648G=