Canonical Allele Identifier: CA392032132
Community Standard Title: NM_138477.4(CDAN1):c.3043C>A (p.Arg1015Ser)
Gene: CDAN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42727674G>T , CM000677.2:g.42727674G>T GRCh38
NC_000015.9:g.43019872G>T , CM000677.1:g.43019872G>T GRCh37
NC_000015.8:g.40807164G>T NCBI36
NG_012491.1:g.14546C>A

Transcript Alleles

HGVS Amino-acid Change
NM_138477.4:c.3043C>A MANE Select NP_612486.2:p.Arg1015Ser
ENST00000356231.4:c.3043C>A MANE Select ENSP00000348564.3:p.Arg1015Ser
NM_138477.2:c.3043C>A NP_612486.2:p.Arg1015Ser
ENST00000356231.3:c.3043C>A ENSP00000348564.3:p.Arg1015Ser
ENST00000562465.5:c.1036C>A ENSP00000454246.1:p.Arg346Ser
ENST00000643434.1:c.*2221C>A ENSP00000494699.1:n.*2221C>A
XM_005254176.3:c.3046C>A XP_005254233.1:p.Arg1016Ser
XM_005254176.5:c.3046C>A XP_005254233.1:p.Arg1016Ser
XM_011521270.1:c.3070C>A XP_011519572.1:p.Arg1024Ser
XM_011521270.2:c.3070C>A XP_011519572.1:p.Arg1024Ser
XM_011521271.1:c.3067C>A XP_011519573.1:p.Arg1023Ser
XM_011521271.2:c.3067C>A XP_011519573.1:p.Arg1023Ser
XM_011521272.1:c.3070C>A XP_011519574.1:p.Arg1024Ser
XM_011521273.1:c.3070C>A XP_011519575.1:p.Arg1024Ser
XM_011521274.1:c.2035C>A XP_011519576.1:p.Arg679Ser
XM_011521274.2:c.2035C>A XP_011519576.1:p.Arg679Ser
XM_011521275.1:c.2287C>A XP_011519577.1:p.Arg763Ser
XR_001751104.1:n.3100C>A
XR_001751105.1:n.3100C>A