Canonical Allele Identifier: CA392042203
Gene: CDAN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42730641C>T , CM000677.2:g.42730641C>T GRCh38
NC_000015.9:g.43022839C>T , CM000677.1:g.43022839C>T GRCh37
NC_000015.8:g.40810131C>T NCBI36
NG_012491.1:g.11579G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356231.4:c.2131G>A MANE Select ENSP00000348564.3:p.Glu711Lys
ENST00000643434.1:c.*1309G>A ENSP00000494699.1:n.*1309G>A
ENST00000356231.3:c.2131G>A ENSP00000348564.3:p.Glu711Lys
ENST00000562465.5:c.124G>A ENSP00000454246.1:p.Glu42Lys
NM_138477.2:c.2131G>A NP_612486.2:p.Glu711Lys
XM_005254176.3:c.2134G>A XP_005254233.1:p.Glu712Lys
XM_011521270.1:c.2158G>A XP_011519572.1:p.Glu720Lys
XM_011521271.1:c.2155G>A XP_011519573.1:p.Glu719Lys
XM_011521272.1:c.2158G>A XP_011519574.1:p.Glu720Lys
XM_011521273.1:c.2158G>A XP_011519575.1:p.Glu720Lys
XM_011521274.1:c.1123G>A XP_011519576.1:p.Glu375Lys
XM_011521275.1:c.1375G>A XP_011519577.1:p.Glu459Lys
XR_931757.1:n.2131G>A
NM_138477.4:c.2131G>A MANE Select NP_612486.2:p.Glu711Lys
XM_005254176.5:c.2134G>A XP_005254233.1:p.Glu712Lys
XM_011521270.2:c.2158G>A XP_011519572.1:p.Glu720Lys
XM_011521271.2:c.2155G>A XP_011519573.1:p.Glu719Lys
XM_011521274.2:c.1123G>A XP_011519576.1:p.Glu375Lys
XR_001751104.1:n.2188G>A
XR_001751105.1:n.2188G>A
XR_931757.2:n.2151G>A