Canonical Allele Identifier: CA7515971
Gene: CDAN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42731654C>G , CM000677.2:g.42731654C>G GRCh38
NC_000015.9:g.43023852C>G , CM000677.1:g.43023852C>G GRCh37
NC_000015.8:g.40811144C>G NCBI36
NG_012491.1:g.10566G>C

Transcript Alleles

HGVS Amino-acid Change
NM_138477.4:c.1705G>C MANE Select NP_612486.2:p.Gly569Arg
ENST00000356231.4:c.1705G>C MANE Select ENSP00000348564.3:p.Gly569Arg
NM_138477.2:c.1705G>C NP_612486.2:p.Gly569Arg
ENST00000356231.3:c.1705G>C ENSP00000348564.3:p.Gly569Arg
ENST00000643434.1:c.*883G>C ENSP00000494699.1:n.*883G>C
XM_005254176.3:c.1708G>C XP_005254233.1:p.Gly570Arg
XM_005254176.5:c.1708G>C XP_005254233.1:p.Gly570Arg
XM_011521270.1:c.1732G>C XP_011519572.1:p.Gly578Arg
XM_011521270.2:c.1732G>C XP_011519572.1:p.Gly578Arg
XM_011521271.1:c.1729G>C XP_011519573.1:p.Gly577Arg
XM_011521271.2:c.1729G>C XP_011519573.1:p.Gly577Arg
XM_011521272.1:c.1732G>C XP_011519574.1:p.Gly578Arg
XM_011521273.1:c.1732G>C XP_011519575.1:p.Gly578Arg
XM_011521274.1:c.697G>C XP_011519576.1:p.Gly233Arg
XM_011521274.2:c.697G>C XP_011519576.1:p.Gly233Arg
XM_011521275.1:c.949G>C XP_011519577.1:p.Gly317Arg
XR_001751104.1:n.1762G>C
XR_001751105.1:n.1762G>C
XR_931757.1:n.1743G>C
XR_931757.2:n.1763G>C