Canonical Allele Identifier: CA392027936
Gene: CDAN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42725610G>C , CM000677.2:g.42725610G>C GRCh38
NC_000015.9:g.43017808G>C , CM000677.1:g.43017808G>C GRCh37
NC_000015.8:g.40805100G>C NCBI36
NG_012491.1:g.16610C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356231.4:c.3329C>G MANE Select ENSP00000348564.3:p.Ala1110Gly
ENST00000643434.1:c.*2396C>G ENSP00000494699.1:n.*2396C>G
ENST00000356231.3:c.3329C>G ENSP00000348564.3:p.Ala1110Gly
ENST00000562465.5:c.1275C>G ENSP00000454246.1:n.1275C>G
ENST00000563604.1:n.28C>G
NM_138477.2:c.3329C>G NP_612486.2:p.Ala1110Gly
XM_005254176.3:c.3332C>G XP_005254233.1:p.Ala1111Gly
XM_011521270.1:c.3356C>G XP_011519572.1:p.Ala1119Gly
XM_011521271.1:c.3353C>G XP_011519573.1:p.Ala1118Gly
XM_011521272.1:c.*37C>G XP_011519574.1:n.*37C>G
XM_011521274.1:c.2321C>G XP_011519576.1:p.Ala774Gly
XM_011521275.1:c.2573C>G XP_011519577.1:p.Ala858Gly
NM_138477.4:c.3329C>G MANE Select NP_612486.2:p.Ala1110Gly
XM_005254176.5:c.3332C>G XP_005254233.1:p.Ala1111Gly
XM_011521270.2:c.3356C>G XP_011519572.1:p.Ala1119Gly
XM_011521271.2:c.3353C>G XP_011519573.1:p.Ala1118Gly
XM_011521274.2:c.2321C>G XP_011519576.1:p.Ala774Gly
XR_001751104.1:n.3322C>G
XR_001751105.1:n.3339C>G