Canonical Allele Identifier: CA392040275
Gene: CDAN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42730191A>C , CM000677.2:g.42730191A>C GRCh38
NC_000015.9:g.43022389A>C , CM000677.1:g.43022389A>C GRCh37
NC_000015.8:g.40809681A>C NCBI36
NG_012491.1:g.12029T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356231.4:c.2199T>G MANE Select ENSP00000348564.3:p.Ser733Arg
ENST00000643434.1:c.*1377T>G ENSP00000494699.1:n.*1377T>G
ENST00000356231.3:c.2199T>G ENSP00000348564.3:p.Ser733Arg
ENST00000562465.5:c.192T>G ENSP00000454246.1:p.Ser64Arg
NM_138477.2:c.2199T>G NP_612486.2:p.Ser733Arg
XM_005254176.3:c.2202T>G XP_005254233.1:p.Ser734Arg
XM_011521270.1:c.2226T>G XP_011519572.1:p.Ser742Arg
XM_011521271.1:c.2223T>G XP_011519573.1:p.Ser741Arg
XM_011521272.1:c.2226T>G XP_011519574.1:p.Ser742Arg
XM_011521273.1:c.2226T>G XP_011519575.1:p.Ser742Arg
XM_011521274.1:c.1191T>G XP_011519576.1:p.Ser397Arg
XM_011521275.1:c.1443T>G XP_011519577.1:p.Ser481Arg
XR_931757.1:n.2199T>G
NM_138477.4:c.2199T>G MANE Select NP_612486.2:p.Ser733Arg
XM_005254176.5:c.2202T>G XP_005254233.1:p.Ser734Arg
XM_011521270.2:c.2226T>G XP_011519572.1:p.Ser742Arg
XM_011521271.2:c.2223T>G XP_011519573.1:p.Ser741Arg
XM_011521274.2:c.1191T>G XP_011519576.1:p.Ser397Arg
XR_001751104.1:n.2256T>G
XR_001751105.1:n.2256T>G
XR_931757.2:n.2219T>G