Canonical Allele Identifier: CA7515398
Gene: CDAN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42728030G>A , CM000677.2:g.42728030G>A GRCh38
NC_000015.9:g.43020228G>A , CM000677.1:g.43020228G>A GRCh37
NC_000015.8:g.40807520G>A NCBI36
NG_012491.1:g.14190C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356231.4:c.2872C>T MANE Select ENSP00000348564.3:p.Leu958=
ENST00000643434.1:c.*2050C>T ENSP00000494699.1:n.*2050C>T
ENST00000356231.3:c.2872C>T ENSP00000348564.3:p.Leu958=
ENST00000562465.5:c.865C>T ENSP00000454246.1:p.Leu289=
NM_138477.2:c.2872C>T NP_612486.2:p.Leu958=
XM_005254176.3:c.2875C>T XP_005254233.1:p.Leu959=
XM_011521270.1:c.2899C>T XP_011519572.1:p.Leu967=
XM_011521271.1:c.2896C>T XP_011519573.1:p.Leu966=
XM_011521272.1:c.2899C>T XP_011519574.1:p.Leu967=
XM_011521273.1:c.2899C>T XP_011519575.1:p.Leu967=
XM_011521274.1:c.1864C>T XP_011519576.1:p.Leu622=
XM_011521275.1:c.2116C>T XP_011519577.1:p.Leu706=
NM_138477.4:c.2872C>T MANE Select NP_612486.2:p.Leu958=
XM_005254176.5:c.2875C>T XP_005254233.1:p.Leu959=
XM_011521270.2:c.2899C>T XP_011519572.1:p.Leu967=
XM_011521271.2:c.2896C>T XP_011519573.1:p.Leu966=
XM_011521274.2:c.1864C>T XP_011519576.1:p.Leu622=
XR_001751104.1:n.2929C>T
XR_001751105.1:n.2929C>T