Canonical Allele Identifier: CA2172870517
Gene: CDAN1 HGNC NCBI

Linked Data

dbSNP Id: rs2061611043

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42731492del , CM000677.2:g.42731492del GRCh38
NC_000015.9:g.43023690del , CM000677.1:g.43023690del GRCh37
NC_000015.8:g.40810982del NCBI36
NG_012491.1:g.10729del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356231.4:c.1739+129del MANE Select ENSP00000348564.3:n.1739+129del
ENST00000643434.1:c.*917+129del ENSP00000494699.1:n.*917+129del
ENST00000356231.3:c.1739+129del ENSP00000348564.3:n.1739+129del
NM_138477.2:c.1739+129del NP_612486.2:n.1739+129del
XM_005254176.3:c.1742+129del XP_005254233.1:n.1742+129del
XM_011521270.1:c.1766+129del XP_011519572.1:n.1766+129del
XM_011521271.1:c.1763+129del XP_011519573.1:n.1763+129del
XM_011521272.1:c.1766+129del XP_011519574.1:n.1766+129del
XM_011521273.1:c.1766+129del XP_011519575.1:n.1766+129del
XM_011521274.1:c.731+129del XP_011519576.1:n.731+129del
XM_011521275.1:c.983+129del XP_011519577.1:n.983+129del
XR_931757.1:n.1777+129del
NM_138477.4:c.1739+129del MANE Select NP_612486.2:n.1739+129del
XM_005254176.5:c.1742+129del XP_005254233.1:n.1742+129del
XM_011521270.2:c.1766+129del XP_011519572.1:n.1766+129del
XM_011521271.2:c.1763+129del XP_011519573.1:n.1763+129del
XM_011521274.2:c.731+129del XP_011519576.1:n.731+129del
XR_001751104.1:n.1796+129del
XR_001751105.1:n.1796+129del
XR_931757.2:n.1797+129del