Canonical Allele Identifier: CA7515873
Gene: CDAN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42730968G>A , CM000677.2:g.42730968G>A GRCh38
NC_000015.9:g.43023166G>A , CM000677.1:g.43023166G>A GRCh37
NC_000015.8:g.40810458G>A NCBI36
NG_012491.1:g.11252C>T

Transcript Alleles

HGVS Amino-acid Change
NM_138477.4:c.1964C>T MANE Select NP_612486.2:p.Pro655Leu
ENST00000356231.4:c.1964C>T MANE Select ENSP00000348564.3:p.Pro655Leu
NM_138477.2:c.1964C>T NP_612486.2:p.Pro655Leu
ENST00000356231.3:c.1964C>T ENSP00000348564.3:p.Pro655Leu
ENST00000643434.1:c.*1142C>T ENSP00000494699.1:n.*1142C>T
XM_005254176.3:c.1967C>T XP_005254233.1:p.Pro656Leu
XM_005254176.5:c.1967C>T XP_005254233.1:p.Pro656Leu
XM_011521270.1:c.1991C>T XP_011519572.1:p.Pro664Leu
XM_011521270.2:c.1991C>T XP_011519572.1:p.Pro664Leu
XM_011521271.1:c.1988C>T XP_011519573.1:p.Pro663Leu
XM_011521271.2:c.1988C>T XP_011519573.1:p.Pro663Leu
XM_011521272.1:c.1991C>T XP_011519574.1:p.Pro664Leu
XM_011521273.1:c.1991C>T XP_011519575.1:p.Pro664Leu
XM_011521274.1:c.956C>T XP_011519576.1:p.Pro319Leu
XM_011521274.2:c.956C>T XP_011519576.1:p.Pro319Leu
XM_011521275.1:c.1208C>T XP_011519577.1:p.Pro403Leu
XR_001751104.1:n.2021C>T
XR_001751105.1:n.2021C>T
XR_931757.1:n.2002C>T
XR_931757.2:n.2022C>T