Canonical Allele Identifier: CA2628073915
Gene: CDAN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42731390T>C , CM000677.2:g.42731390T>C GRCh38
NC_000015.9:g.43023588T>C , CM000677.1:g.43023588T>C GRCh37
NC_000015.8:g.40810880T>C NCBI36
NG_012491.1:g.10830A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356231.4:c.1740-59A>G MANE Select ENSP00000348564.3:n.1740-59A>G
ENST00000643434.1:c.*918-59A>G ENSP00000494699.1:n.*918-59A>G
ENST00000356231.3:c.1740-59A>G ENSP00000348564.3:n.1740-59A>G
NM_138477.2:c.1740-59A>G NP_612486.2:n.1740-59A>G
XM_005254176.3:c.1743-59A>G XP_005254233.1:n.1743-59A>G
XM_011521270.1:c.1767-59A>G XP_011519572.1:n.1767-59A>G
XM_011521271.1:c.1764-59A>G XP_011519573.1:n.1764-59A>G
XM_011521272.1:c.1767-59A>G XP_011519574.1:n.1767-59A>G
XM_011521273.1:c.1767-59A>G XP_011519575.1:n.1767-59A>G
XM_011521274.1:c.732-59A>G XP_011519576.1:n.732-59A>G
XM_011521275.1:c.984-59A>G XP_011519577.1:n.984-59A>G
XR_931757.1:n.1778-59A>G
NM_138477.4:c.1740-59A>G MANE Select NP_612486.2:n.1740-59A>G
XM_005254176.5:c.1743-59A>G XP_005254233.1:n.1743-59A>G
XM_011521270.2:c.1767-59A>G XP_011519572.1:n.1767-59A>G
XM_011521271.2:c.1764-59A>G XP_011519573.1:n.1764-59A>G
XM_011521274.2:c.732-59A>G XP_011519576.1:n.732-59A>G
XR_001751104.1:n.1797-59A>G
XR_001751105.1:n.1797-59A>G
XR_931757.2:n.1798-59A>G