Canonical Allele Identifier: CA392042221
Gene: CDAN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42730644G>T , CM000677.2:g.42730644G>T GRCh38
NC_000015.9:g.43022842G>T , CM000677.1:g.43022842G>T GRCh37
NC_000015.8:g.40810134G>T NCBI36
NG_012491.1:g.11576C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000356231.4:c.2128C>A MANE Select ENSP00000348564.3:p.Leu710Met
ENST00000643434.1:c.*1306C>A ENSP00000494699.1:n.*1306C>A
ENST00000356231.3:c.2128C>A ENSP00000348564.3:p.Leu710Met
ENST00000562465.5:c.121C>A ENSP00000454246.1:p.Leu41Met
NM_138477.2:c.2128C>A NP_612486.2:p.Leu710Met
XM_005254176.3:c.2131C>A XP_005254233.1:p.Leu711Met
XM_011521270.1:c.2155C>A XP_011519572.1:p.Leu719Met
XM_011521271.1:c.2152C>A XP_011519573.1:p.Leu718Met
XM_011521272.1:c.2155C>A XP_011519574.1:p.Leu719Met
XM_011521273.1:c.2155C>A XP_011519575.1:p.Leu719Met
XM_011521274.1:c.1120C>A XP_011519576.1:p.Leu374Met
XM_011521275.1:c.1372C>A XP_011519577.1:p.Leu458Met
XR_931757.1:n.2128C>A
NM_138477.4:c.2128C>A MANE Select NP_612486.2:p.Leu710Met
XM_005254176.5:c.2131C>A XP_005254233.1:p.Leu711Met
XM_011521270.2:c.2155C>A XP_011519572.1:p.Leu719Met
XM_011521271.2:c.2152C>A XP_011519573.1:p.Leu718Met
XM_011521274.2:c.1120C>A XP_011519576.1:p.Leu374Met
XR_001751104.1:n.2185C>A
XR_001751105.1:n.2185C>A
XR_931757.2:n.2148C>A