Canonical Allele Identifier: CA10635991
Gene: CDAN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42724433C>T , CM000677.2:g.42724433C>T GRCh38
NC_000015.9:g.43016631C>T , CM000677.1:g.43016631C>T GRCh37
NC_000015.8:g.40803923C>T NCBI36
NG_012491.1:g.17787G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356231.4:c.*58G>A MANE Select ENSP00000348564.3:n.*58G>A
ENST00000643434.1:c.*2809G>A ENSP00000494699.1:n.*2809G>A
ENST00000356231.3:c.*58G>A ENSP00000348564.3:n.*58G>A
ENST00000562465.5:c.1688G>A ENSP00000454246.1:n.1688G>A
ENST00000563604.1:n.1205G>A
NM_138477.2:c.*58G>A NP_612486.2:n.*58G>A
XM_005254176.3:c.*58G>A XP_005254233.1:n.*58G>A
XM_011521270.1:c.*58G>A XP_011519572.1:n.*58G>A
XM_011521271.1:c.*58G>A XP_011519573.1:n.*58G>A
XM_011521274.1:c.*58G>A XP_011519576.1:n.*58G>A
XM_011521275.1:c.*58G>A XP_011519577.1:n.*58G>A
NM_138477.4:c.*58G>A MANE Select NP_612486.2:n.*58G>A
XM_005254176.5:c.*58G>A XP_005254233.1:n.*58G>A
XM_011521270.2:c.*58G>A XP_011519572.1:n.*58G>A
XM_011521271.2:c.*58G>A XP_011519573.1:n.*58G>A
XM_011521274.2:c.*58G>A XP_011519576.1:n.*58G>A
XR_001751104.1:n.3735G>A
XR_001751105.1:n.3752G>A