Canonical Allele Identifier: CA7516034

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42732373_42732378dup , CM000677.2:g.42732373_42732378dup	GRCh38
NC_000015.9:g.43024571_43024576dup , CM000677.1:g.43024571_43024576dup	GRCh37
NC_000015.8:g.40811863_40811868dup	NCBI36
NG_012491.1:g.9849_9854dup

Transcript Alleles

HGVS	Amino-acid Change
NM_138477.4:c.1495_1500dup MANE Select	NP_612486.2:p.His500_Phe501insSerHis
ENST00000356231.4:c.1495_1500dup MANE Select	ENSP00000348564.3:p.His500_Phe501insSerHis
NM_138477.2:c.1495_1500dup	NP_612486.2:p.His500_Phe501insSerHis
ENST00000356231.3:c.1495_1500dup	ENSP00000348564.3:p.His500_Phe501insSerHis
ENST00000643434.1:c.*673_*678dup	ENSP00000494699.1:n.*673_*678dup
XM_005254176.3:c.1498_1503dup	XP_005254233.1:p.His501_Phe502insSerHis
XM_005254176.5:c.1498_1503dup	XP_005254233.1:p.His501_Phe502insSerHis
XM_011521270.1:c.1522_1527dup	XP_011519572.1:p.His509_Phe510insSerHis
XM_011521270.2:c.1522_1527dup	XP_011519572.1:p.His509_Phe510insSerHis
XM_011521271.1:c.1519_1524dup	XP_011519573.1:p.His508_Phe509insSerHis
XM_011521271.2:c.1519_1524dup	XP_011519573.1:p.His508_Phe509insSerHis
XM_011521272.1:c.1522_1527dup	XP_011519574.1:p.His509_Phe510insSerHis
XM_011521273.1:c.1522_1527dup	XP_011519575.1:p.His509_Phe510insSerHis
XM_011521274.1:c.487_492dup	XP_011519576.1:p.His164_Phe165insSerHis
XM_011521274.2:c.487_492dup	XP_011519576.1:p.His164_Phe165insSerHis
XM_011521275.1:c.739_744dup	XP_011519577.1:p.His248_Phe249insSerHis
XR_001751104.1:n.1552_1557dup
XR_001751105.1:n.1552_1557dup
XR_931757.1:n.1533_1538dup
XR_931757.2:n.1553_1558dup