Canonical Allele Identifier: CA392044257
Gene: CDAN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42731209A>T , CM000677.2:g.42731209A>T GRCh38
NC_000015.9:g.43023407A>T , CM000677.1:g.43023407A>T GRCh37
NC_000015.8:g.40810699A>T NCBI36
NG_012491.1:g.11011T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000356231.4:c.1860+2T>A MANE Select ENSP00000348564.3:n.1860+2T>A
ENST00000643434.1:c.*1038+2T>A ENSP00000494699.1:n.*1038+2T>A
ENST00000356231.3:c.1860+2T>A ENSP00000348564.3:n.1860+2T>A
NM_138477.2:c.1860+2T>A NP_612486.2:n.1860+2T>A
XM_005254176.3:c.1863+2T>A XP_005254233.1:n.1863+2T>A
XM_011521270.1:c.1887+2T>A XP_011519572.1:n.1887+2T>A
XM_011521271.1:c.1884+2T>A XP_011519573.1:n.1884+2T>A
XM_011521272.1:c.1887+2T>A XP_011519574.1:n.1887+2T>A
XM_011521273.1:c.1887+2T>A XP_011519575.1:n.1887+2T>A
XM_011521274.1:c.852+2T>A XP_011519576.1:n.852+2T>A
XM_011521275.1:c.1104+2T>A XP_011519577.1:n.1104+2T>A
XR_931757.1:n.1898+2T>A
NM_138477.4:c.1860+2T>A MANE Select NP_612486.2:n.1860+2T>A
XM_005254176.5:c.1863+2T>A XP_005254233.1:n.1863+2T>A
XM_011521270.2:c.1887+2T>A XP_011519572.1:n.1887+2T>A
XM_011521271.2:c.1884+2T>A XP_011519573.1:n.1884+2T>A
XM_011521274.2:c.852+2T>A XP_011519576.1:n.852+2T>A
XR_001751104.1:n.1917+2T>A
XR_001751105.1:n.1917+2T>A
XR_931757.2:n.1918+2T>A