Canonical Allele Identifier: CA2172869142
Gene: CDAN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42728985G= , CM000677.2:g.42728985G= GRCh38
NC_000015.9:g.43021183G= , CM000677.1:g.43021183G= GRCh37
NC_000015.8:g.40808475G= NCBI36
NG_012491.1:g.13235C=

Transcript Alleles

HGVS Amino-acid change
ENST00000356231.4:c.2645+38C= MANE Select ENSP00000348564.3:n.2645+38C=
ENST00000643434.1:c.*1823+38C= ENSP00000494699.1:n.*1823+38C=
ENST00000356231.3:c.2645+38C= ENSP00000348564.3:n.2645+38C=
ENST00000562465.5:c.638+38C= ENSP00000454246.1:n.638+38C=
NM_138477.2:c.2645+38C= NP_612486.2:n.2645+38C=
XM_005254176.3:c.2648+38C= XP_005254233.1:n.2648+38C=
XM_011521270.1:c.2672+38C= XP_011519572.1:n.2672+38C=
XM_011521271.1:c.2669+38C= XP_011519573.1:n.2669+38C=
XM_011521272.1:c.2672+38C= XP_011519574.1:n.2672+38C=
XM_011521273.1:c.2672+38C= XP_011519575.1:n.2672+38C=
XM_011521274.1:c.1637+38C= XP_011519576.1:n.1637+38C=
XM_011521275.1:c.1889+38C= XP_011519577.1:n.1889+38C=
NM_138477.4:c.2645+38C= MANE Select NP_612486.2:n.2645+38C=
XM_005254176.5:c.2648+38C= XP_005254233.1:n.2648+38C=
XM_011521270.2:c.2672+38C= XP_011519572.1:n.2672+38C=
XM_011521271.2:c.2669+38C= XP_011519573.1:n.2669+38C=
XM_011521274.2:c.1637+38C= XP_011519576.1:n.1637+38C=
XR_001751104.1:n.2702+38C=
XR_001751105.1:n.2702+38C=