Canonical Allele Identifier: CA2172867528

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42726390G= , CM000677.2:g.42726390G=	GRCh38
NC_000015.9:g.43018588G= , CM000677.1:g.43018588G=	GRCh37
NC_000015.8:g.40805880G=	NCBI36
NG_012491.1:g.15830C=

Transcript Alleles

HGVS	Amino-acid Change
NM_138477.4:c.3124C= MANE Select	NP_612486.2:p.Arg1042=
ENST00000356231.4:c.3124C= MANE Select	ENSP00000348564.3:p.Arg1042=
NM_138477.2:c.3124C=	NP_612486.2:p.Arg1042=
ENST00000356231.3:c.3124C=	ENSP00000348564.3:p.Arg1042=
ENST00000562465.5:c.1070C=	ENSP00000454246.1:n.1070C=
ENST00000643434.1:c.*2255C=	ENSP00000494699.1:n.*2255C=
XM_005254176.3:c.3127C=	XP_005254233.1:p.Arg1043=
XM_005254176.5:c.3127C=	XP_005254233.1:p.Arg1043=
XM_011521270.1:c.3151C=	XP_011519572.1:p.Arg1051=
XM_011521270.2:c.3151C=	XP_011519572.1:p.Arg1051=
XM_011521271.1:c.3148C=	XP_011519573.1:p.Arg1050=
XM_011521271.2:c.3148C=	XP_011519573.1:p.Arg1050=
XM_011521272.1:c.3151C=	XP_011519574.1:p.Arg1051=
XM_011521273.1:c.*26C=	XP_011519575.1:n.*26C=
XM_011521274.1:c.2116C=	XP_011519576.1:p.Arg706=
XM_011521274.2:c.2116C=	XP_011519576.1:p.Arg706=
XM_011521275.1:c.2368C=	XP_011519577.1:p.Arg790=
XR_001751104.1:n.3181C=
XR_001751105.1:n.3134C=