Canonical Allele Identifier: CA392044949
Gene: CDAN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42731282C>G , CM000677.2:g.42731282C>G GRCh38
NC_000015.9:g.43023480C>G , CM000677.1:g.43023480C>G GRCh37
NC_000015.8:g.40810772C>G NCBI36
NG_012491.1:g.10938G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000356231.4:c.1789G>C MANE Select ENSP00000348564.3:p.Glu597Gln
ENST00000643434.1:c.*967G>C ENSP00000494699.1:n.*967G>C
ENST00000356231.3:c.1789G>C ENSP00000348564.3:p.Glu597Gln
NM_138477.2:c.1789G>C NP_612486.2:p.Glu597Gln
XM_005254176.3:c.1792G>C XP_005254233.1:p.Glu598Gln
XM_011521270.1:c.1816G>C XP_011519572.1:p.Glu606Gln
XM_011521271.1:c.1813G>C XP_011519573.1:p.Glu605Gln
XM_011521272.1:c.1816G>C XP_011519574.1:p.Glu606Gln
XM_011521273.1:c.1816G>C XP_011519575.1:p.Glu606Gln
XM_011521274.1:c.781G>C XP_011519576.1:p.Glu261Gln
XM_011521275.1:c.1033G>C XP_011519577.1:p.Glu345Gln
XR_931757.1:n.1827G>C
NM_138477.4:c.1789G>C MANE Select NP_612486.2:p.Glu597Gln
XM_005254176.5:c.1792G>C XP_005254233.1:p.Glu598Gln
XM_011521270.2:c.1816G>C XP_011519572.1:p.Glu606Gln
XM_011521271.2:c.1813G>C XP_011519573.1:p.Glu605Gln
XM_011521274.2:c.781G>C XP_011519576.1:p.Glu261Gln
XR_001751104.1:n.1846G>C
XR_001751105.1:n.1846G>C
XR_931757.2:n.1847G>C