Canonical Allele Identifier: CA2628074041
Gene: CDAN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42731561G>A , CM000677.2:g.42731561G>A GRCh38
NC_000015.9:g.43023759G>A , CM000677.1:g.43023759G>A GRCh37
NC_000015.8:g.40811051G>A NCBI36
NG_012491.1:g.10659C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356231.4:c.1739+59C>T MANE Select ENSP00000348564.3:n.1739+59C>T
ENST00000643434.1:c.*917+59C>T ENSP00000494699.1:n.*917+59C>T
ENST00000356231.3:c.1739+59C>T ENSP00000348564.3:n.1739+59C>T
NM_138477.2:c.1739+59C>T NP_612486.2:n.1739+59C>T
XM_005254176.3:c.1742+59C>T XP_005254233.1:n.1742+59C>T
XM_011521270.1:c.1766+59C>T XP_011519572.1:n.1766+59C>T
XM_011521271.1:c.1763+59C>T XP_011519573.1:n.1763+59C>T
XM_011521272.1:c.1766+59C>T XP_011519574.1:n.1766+59C>T
XM_011521273.1:c.1766+59C>T XP_011519575.1:n.1766+59C>T
XM_011521274.1:c.731+59C>T XP_011519576.1:n.731+59C>T
XM_011521275.1:c.983+59C>T XP_011519577.1:n.983+59C>T
XR_931757.1:n.1777+59C>T
NM_138477.4:c.1739+59C>T MANE Select NP_612486.2:n.1739+59C>T
XM_005254176.5:c.1742+59C>T XP_005254233.1:n.1742+59C>T
XM_011521270.2:c.1766+59C>T XP_011519572.1:n.1766+59C>T
XM_011521271.2:c.1763+59C>T XP_011519573.1:n.1763+59C>T
XM_011521274.2:c.731+59C>T XP_011519576.1:n.731+59C>T
XR_001751104.1:n.1796+59C>T
XR_001751105.1:n.1796+59C>T
XR_931757.2:n.1797+59C>T