Canonical Allele Identifier: CA2628073971
Gene: CDAN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42731459_42731469del , CM000677.2:g.42731459_42731469del GRCh38
NC_000015.9:g.43023657_43023667del , CM000677.1:g.43023657_43023667del GRCh37
NC_000015.8:g.40810949_40810959del NCBI36
NG_012491.1:g.10751_10761del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356231.4:c.1740-138_1740-128del MANE Select ENSP00000348564.3:n.1740-138_1740-128del
ENST00000643434.1:c.*918-138_*918-128del ENSP00000494699.1:n.*918-138_*918-128del
ENST00000356231.3:c.1740-138_1740-128del ENSP00000348564.3:n.1740-138_1740-128del
NM_138477.2:c.1740-138_1740-128del NP_612486.2:n.1740-138_1740-128del
XM_005254176.3:c.1743-138_1743-128del XP_005254233.1:n.1743-138_1743-128del
XM_011521270.1:c.1767-138_1767-128del XP_011519572.1:n.1767-138_1767-128del
XM_011521271.1:c.1764-138_1764-128del XP_011519573.1:n.1764-138_1764-128del
XM_011521272.1:c.1767-138_1767-128del XP_011519574.1:n.1767-138_1767-128del
XM_011521273.1:c.1767-138_1767-128del XP_011519575.1:n.1767-138_1767-128del
XM_011521274.1:c.732-138_732-128del XP_011519576.1:n.732-138_732-128del
XM_011521275.1:c.984-138_984-128del XP_011519577.1:n.984-138_984-128del
XR_931757.1:n.1778-138_1778-128del
NM_138477.4:c.1740-138_1740-128del MANE Select NP_612486.2:n.1740-138_1740-128del
XM_005254176.5:c.1743-138_1743-128del XP_005254233.1:n.1743-138_1743-128del
XM_011521270.2:c.1767-138_1767-128del XP_011519572.1:n.1767-138_1767-128del
XM_011521271.2:c.1764-138_1764-128del XP_011519573.1:n.1764-138_1764-128del
XM_011521274.2:c.732-138_732-128del XP_011519576.1:n.732-138_732-128del
XR_001751104.1:n.1797-138_1797-128del
XR_001751105.1:n.1797-138_1797-128del
XR_931757.2:n.1798-138_1798-128del