Canonical Allele Identifier: CA392042367
Gene: CDAN1 HGNC NCBI

Linked Data

dbSNP Id: rs1456901791

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42730670G>A , CM000677.2:g.42730670G>A GRCh38
NC_000015.9:g.43022868G>A , CM000677.1:g.43022868G>A GRCh37
NC_000015.8:g.40810160G>A NCBI36
NG_012491.1:g.11550C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000356231.4:c.2102C>T MANE Select ENSP00000348564.3:p.Ser701Phe
ENST00000643434.1:c.*1280C>T ENSP00000494699.1:n.*1280C>T
ENST00000356231.3:c.2102C>T ENSP00000348564.3:p.Ser701Phe
ENST00000562465.5:c.95C>T ENSP00000454246.1:p.Ser32Phe
NM_138477.2:c.2102C>T NP_612486.2:p.Ser701Phe
XM_005254176.3:c.2105C>T XP_005254233.1:p.Ser702Phe
XM_011521270.1:c.2129C>T XP_011519572.1:p.Ser710Phe
XM_011521271.1:c.2126C>T XP_011519573.1:p.Ser709Phe
XM_011521272.1:c.2129C>T XP_011519574.1:p.Ser710Phe
XM_011521273.1:c.2129C>T XP_011519575.1:p.Ser710Phe
XM_011521274.1:c.1094C>T XP_011519576.1:p.Ser365Phe
XM_011521275.1:c.1346C>T XP_011519577.1:p.Ser449Phe
XR_931757.1:n.2102C>T
NM_138477.4:c.2102C>T MANE Select NP_612486.2:p.Ser701Phe
XM_005254176.5:c.2105C>T XP_005254233.1:p.Ser702Phe
XM_011521270.2:c.2129C>T XP_011519572.1:p.Ser710Phe
XM_011521271.2:c.2126C>T XP_011519573.1:p.Ser709Phe
XM_011521274.2:c.1094C>T XP_011519576.1:p.Ser365Phe
XR_001751104.1:n.2159C>T
XR_001751105.1:n.2159C>T
XR_931757.2:n.2122C>T