Canonical Allele Identifier: CA2998951722
Community Standard Title: NM_138477.4(CDAN1):c.2262+6del
Gene: CDAN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42730122del , CM000677.2:g.42730122del GRCh38
NC_000015.9:g.43022320del , CM000677.1:g.43022320del GRCh37
NC_000015.8:g.40809612del NCBI36
NG_012491.1:g.12098del

Transcript Alleles

HGVS Amino-acid Change
NM_138477.4:c.2262+6del MANE Select NP_612486.2:n.2262+6del
ENST00000356231.4:c.2262+6del MANE Select ENSP00000348564.3:n.2262+6del
NM_138477.2:c.2262+6del NP_612486.2:n.2262+6del
ENST00000356231.3:c.2262+6del ENSP00000348564.3:n.2262+6del
ENST00000562465.5:c.255+6del ENSP00000454246.1:n.255+6del
ENST00000643434.1:c.*1440+6del ENSP00000494699.1:n.*1440+6del
XM_005254176.3:c.2265+6del XP_005254233.1:n.2265+6del
XM_005254176.5:c.2265+6del XP_005254233.1:n.2265+6del
XM_011521270.1:c.2289+6del XP_011519572.1:n.2289+6del
XM_011521270.2:c.2289+6del XP_011519572.1:n.2289+6del
XM_011521271.1:c.2286+6del XP_011519573.1:n.2286+6del
XM_011521271.2:c.2286+6del XP_011519573.1:n.2286+6del
XM_011521272.1:c.2289+6del XP_011519574.1:n.2289+6del
XM_011521273.1:c.2289+6del XP_011519575.1:n.2289+6del
XM_011521274.1:c.1254+6del XP_011519576.1:n.1254+6del
XM_011521274.2:c.1254+6del XP_011519576.1:n.1254+6del
XM_011521275.1:c.1506+6del XP_011519577.1:n.1506+6del
XR_001751104.1:n.2319+6del
XR_001751105.1:n.2319+6del