Canonical Allele Identifier: CA7515468
Community Standard Title: NM_138477.4(CDAN1):c.2801G>A (p.Arg934Gln)
Gene: CDAN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42728655C>T , CM000677.2:g.42728655C>T GRCh38
NC_000015.9:g.43020853C>T , CM000677.1:g.43020853C>T GRCh37
NC_000015.8:g.40808145C>T NCBI36
NG_012491.1:g.13565G>A

Transcript Alleles

HGVS Amino-acid Change
NM_138477.4:c.2801G>A MANE Select NP_612486.2:p.Arg934Gln
ENST00000356231.4:c.2801G>A MANE Select ENSP00000348564.3:p.Arg934Gln
NM_138477.2:c.2801G>A NP_612486.2:p.Arg934Gln
ENST00000356231.3:c.2801G>A ENSP00000348564.3:p.Arg934Gln
ENST00000562465.5:c.794G>A ENSP00000454246.1:p.Arg265Gln
ENST00000643434.1:c.*1979G>A ENSP00000494699.1:n.*1979G>A
XM_005254176.3:c.2804G>A XP_005254233.1:p.Arg935Gln
XM_005254176.5:c.2804G>A XP_005254233.1:p.Arg935Gln
XM_011521270.1:c.2828G>A XP_011519572.1:p.Arg943Gln
XM_011521270.2:c.2828G>A XP_011519572.1:p.Arg943Gln
XM_011521271.1:c.2825G>A XP_011519573.1:p.Arg942Gln
XM_011521271.2:c.2825G>A XP_011519573.1:p.Arg942Gln
XM_011521272.1:c.2828G>A XP_011519574.1:p.Arg943Gln
XM_011521273.1:c.2828G>A XP_011519575.1:p.Arg943Gln
XM_011521274.1:c.1793G>A XP_011519576.1:p.Arg598Gln
XM_011521274.2:c.1793G>A XP_011519576.1:p.Arg598Gln
XM_011521275.1:c.2045G>A XP_011519577.1:p.Arg682Gln
XR_001751104.1:n.2858G>A
XR_001751105.1:n.2858G>A