Canonical Allele Identifier: CA392044802
Gene: CDAN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42731263A>T , CM000677.2:g.42731263A>T GRCh38
NC_000015.9:g.43023461A>T , CM000677.1:g.43023461A>T GRCh37
NC_000015.8:g.40810753A>T NCBI36
NG_012491.1:g.10957T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356231.4:c.1808T>A MANE Select ENSP00000348564.3:p.Leu603Gln
ENST00000643434.1:c.*986T>A ENSP00000494699.1:n.*986T>A
ENST00000356231.3:c.1808T>A ENSP00000348564.3:p.Leu603Gln
NM_138477.2:c.1808T>A NP_612486.2:p.Leu603Gln
XM_005254176.3:c.1811T>A XP_005254233.1:p.Leu604Gln
XM_011521270.1:c.1835T>A XP_011519572.1:p.Leu612Gln
XM_011521271.1:c.1832T>A XP_011519573.1:p.Leu611Gln
XM_011521272.1:c.1835T>A XP_011519574.1:p.Leu612Gln
XM_011521273.1:c.1835T>A XP_011519575.1:p.Leu612Gln
XM_011521274.1:c.800T>A XP_011519576.1:p.Leu267Gln
XM_011521275.1:c.1052T>A XP_011519577.1:p.Leu351Gln
XR_931757.1:n.1846T>A
NM_138477.4:c.1808T>A MANE Select NP_612486.2:p.Leu603Gln
XM_005254176.5:c.1811T>A XP_005254233.1:p.Leu604Gln
XM_011521270.2:c.1835T>A XP_011519572.1:p.Leu612Gln
XM_011521271.2:c.1832T>A XP_011519573.1:p.Leu611Gln
XM_011521274.2:c.800T>A XP_011519576.1:p.Leu267Gln
XR_001751104.1:n.1865T>A
XR_001751105.1:n.1865T>A
XR_931757.2:n.1866T>A