Canonical Allele Identifier: CA2172870388

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731249G= , CM000677.2:g.42731249G=	GRCh38
NC_000015.9:g.43023447G= , CM000677.1:g.43023447G=	GRCh37
NC_000015.8:g.40810739G=	NCBI36
NG_012491.1:g.10971C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1822C= MANE Select	ENSP00000348564.3:p.Pro608=
ENST00000643434.1:c.*1000C=	ENSP00000494699.1:n.*1000C=
ENST00000356231.3:c.1822C=	ENSP00000348564.3:p.Pro608=
NM_138477.2:c.1822C=	NP_612486.2:p.Pro608=
XM_005254176.3:c.1825C=	XP_005254233.1:p.Pro609=
XM_011521270.1:c.1849C=	XP_011519572.1:p.Pro617=
XM_011521271.1:c.1846C=	XP_011519573.1:p.Pro616=
XM_011521272.1:c.1849C=	XP_011519574.1:p.Pro617=
XM_011521273.1:c.1849C=	XP_011519575.1:p.Pro617=
XM_011521274.1:c.814C=	XP_011519576.1:p.Pro272=
XM_011521275.1:c.1066C=	XP_011519577.1:p.Pro356=
XR_931757.1:n.1860C=
NM_138477.4:c.1822C= MANE Select	NP_612486.2:p.Pro608=
XM_005254176.5:c.1825C=	XP_005254233.1:p.Pro609=
XM_011521270.2:c.1849C=	XP_011519572.1:p.Pro617=
XM_011521271.2:c.1846C=	XP_011519573.1:p.Pro616=
XM_011521274.2:c.814C=	XP_011519576.1:p.Pro272=
XR_001751104.1:n.1879C=
XR_001751105.1:n.1879C=
XR_931757.2:n.1880C=