Canonical Allele Identifier: CA392042365
Gene: CDAN1 HGNC NCBI

Linked Data

dbSNP Id: rs1456901791

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42730670G>C , CM000677.2:g.42730670G>C GRCh38
NC_000015.9:g.43022868G>C , CM000677.1:g.43022868G>C GRCh37
NC_000015.8:g.40810160G>C NCBI36
NG_012491.1:g.11550C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000356231.4:c.2102C>G MANE Select ENSP00000348564.3:p.Ser701Cys
ENST00000643434.1:c.*1280C>G ENSP00000494699.1:n.*1280C>G
ENST00000356231.3:c.2102C>G ENSP00000348564.3:p.Ser701Cys
ENST00000562465.5:c.95C>G ENSP00000454246.1:p.Ser32Cys
NM_138477.2:c.2102C>G NP_612486.2:p.Ser701Cys
XM_005254176.3:c.2105C>G XP_005254233.1:p.Ser702Cys
XM_011521270.1:c.2129C>G XP_011519572.1:p.Ser710Cys
XM_011521271.1:c.2126C>G XP_011519573.1:p.Ser709Cys
XM_011521272.1:c.2129C>G XP_011519574.1:p.Ser710Cys
XM_011521273.1:c.2129C>G XP_011519575.1:p.Ser710Cys
XM_011521274.1:c.1094C>G XP_011519576.1:p.Ser365Cys
XM_011521275.1:c.1346C>G XP_011519577.1:p.Ser449Cys
XR_931757.1:n.2102C>G
NM_138477.4:c.2102C>G MANE Select NP_612486.2:p.Ser701Cys
XM_005254176.5:c.2105C>G XP_005254233.1:p.Ser702Cys
XM_011521270.2:c.2129C>G XP_011519572.1:p.Ser710Cys
XM_011521271.2:c.2126C>G XP_011519573.1:p.Ser709Cys
XM_011521274.2:c.1094C>G XP_011519576.1:p.Ser365Cys
XR_001751104.1:n.2159C>G
XR_001751105.1:n.2159C>G
XR_931757.2:n.2122C>G