Canonical Allele Identifier: CA2172870557

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731581G= , CM000677.2:g.42731581G=	GRCh38
NC_000015.9:g.43023779G= , CM000677.1:g.43023779G=	GRCh37
NC_000015.8:g.40811071G=	NCBI36
NG_012491.1:g.10639C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1739+39C= MANE Select	ENSP00000348564.3:n.1739+39C=
ENST00000643434.1:c.*917+39C=	ENSP00000494699.1:n.*917+39C=
ENST00000356231.3:c.1739+39C=	ENSP00000348564.3:n.1739+39C=
NM_138477.2:c.1739+39C=	NP_612486.2:n.1739+39C=
XM_005254176.3:c.1742+39C=	XP_005254233.1:n.1742+39C=
XM_011521270.1:c.1766+39C=	XP_011519572.1:n.1766+39C=
XM_011521271.1:c.1763+39C=	XP_011519573.1:n.1763+39C=
XM_011521272.1:c.1766+39C=	XP_011519574.1:n.1766+39C=
XM_011521273.1:c.1766+39C=	XP_011519575.1:n.1766+39C=
XM_011521274.1:c.731+39C=	XP_011519576.1:n.731+39C=
XM_011521275.1:c.983+39C=	XP_011519577.1:n.983+39C=
XR_931757.1:n.1777+39C=
NM_138477.4:c.1739+39C= MANE Select	NP_612486.2:n.1739+39C=
XM_005254176.5:c.1742+39C=	XP_005254233.1:n.1742+39C=
XM_011521270.2:c.1766+39C=	XP_011519572.1:n.1766+39C=
XM_011521271.2:c.1763+39C=	XP_011519573.1:n.1763+39C=
XM_011521274.2:c.731+39C=	XP_011519576.1:n.731+39C=
XR_001751104.1:n.1796+39C=
XR_001751105.1:n.1796+39C=
XR_931757.2:n.1797+39C=