Canonical Allele Identifier: CA489895199
Gene: CDAN1 HGNC NCBI

Linked Data

dbSNP Id: rs2061598421
MyVariant Identifiers: chr15:g.43022837T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42730639T>C , CM000677.2:g.42730639T>C GRCh38
NC_000015.9:g.43022837T>C , CM000677.1:g.43022837T>C GRCh37
NC_000015.8:g.40810129T>C NCBI36
NG_012491.1:g.11581A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356231.4:c.2133A>G MANE Select ENSP00000348564.3:p.Glu711=
ENST00000643434.1:c.*1311A>G ENSP00000494699.1:n.*1311A>G
ENST00000356231.3:c.2133A>G ENSP00000348564.3:p.Glu711=
ENST00000562465.5:c.126A>G ENSP00000454246.1:p.Glu42=
NM_138477.2:c.2133A>G NP_612486.2:p.Glu711=
XM_005254176.3:c.2136A>G XP_005254233.1:p.Glu712=
XM_011521270.1:c.2160A>G XP_011519572.1:p.Glu720=
XM_011521271.1:c.2157A>G XP_011519573.1:p.Glu719=
XM_011521272.1:c.2160A>G XP_011519574.1:p.Glu720=
XM_011521273.1:c.2160A>G XP_011519575.1:p.Glu720=
XM_011521274.1:c.1125A>G XP_011519576.1:p.Glu375=
XM_011521275.1:c.1377A>G XP_011519577.1:p.Glu459=
XR_931757.1:n.2133A>G
NM_138477.4:c.2133A>G MANE Select NP_612486.2:p.Glu711=
XM_005254176.5:c.2136A>G XP_005254233.1:p.Glu712=
XM_011521270.2:c.2160A>G XP_011519572.1:p.Glu720=
XM_011521271.2:c.2157A>G XP_011519573.1:p.Glu719=
XM_011521274.2:c.1125A>G XP_011519576.1:p.Glu375=
XR_001751104.1:n.2190A>G
XR_001751105.1:n.2190A>G
XR_931757.2:n.2153A>G