Canonical Allele Identifier: CA2628073982
Gene: CDAN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42731476_42731479del , CM000677.2:g.42731476_42731479del GRCh38
NC_000015.9:g.43023674_43023677del , CM000677.1:g.43023674_43023677del GRCh37
NC_000015.8:g.40810966_40810969del NCBI36
NG_012491.1:g.10743_10746del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356231.4:c.1739+143_1740-143del MANE Select ENSP00000348564.3:n.1739+143_1740-143del
ENST00000643434.1:c.*917+143_*918-143del ENSP00000494699.1:n.*917+143_*918-143del
ENST00000356231.3:c.1739+143_1740-143del ENSP00000348564.3:n.1739+143_1740-143del
NM_138477.2:c.1739+143_1740-143del NP_612486.2:n.1739+143_1740-143del
XM_005254176.3:c.1742+143_1743-143del XP_005254233.1:n.1742+143_1743-143del
XM_011521270.1:c.1766+143_1767-143del XP_011519572.1:n.1766+143_1767-143del
XM_011521271.1:c.1763+143_1764-143del XP_011519573.1:n.1763+143_1764-143del
XM_011521272.1:c.1766+143_1767-143del XP_011519574.1:n.1766+143_1767-143del
XM_011521273.1:c.1766+143_1767-143del XP_011519575.1:n.1766+143_1767-143del
XM_011521274.1:c.731+143_732-143del XP_011519576.1:n.731+143_732-143del
XM_011521275.1:c.983+143_984-143del XP_011519577.1:n.983+143_984-143del
XR_931757.1:n.1777+143_1778-143del
NM_138477.4:c.1739+143_1740-143del MANE Select NP_612486.2:n.1739+143_1740-143del
XM_005254176.5:c.1742+143_1743-143del XP_005254233.1:n.1742+143_1743-143del
XM_011521270.2:c.1766+143_1767-143del XP_011519572.1:n.1766+143_1767-143del
XM_011521271.2:c.1763+143_1764-143del XP_011519573.1:n.1763+143_1764-143del
XM_011521274.2:c.731+143_732-143del XP_011519576.1:n.731+143_732-143del
XR_001751104.1:n.1796+143_1797-143del
XR_001751105.1:n.1796+143_1797-143del
XR_931757.2:n.1797+143_1798-143del