Canonical Allele Identifier: CA1363291685
Gene: IMPDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026847G= , CM000665.2:g.49026847G= GRCh38
NC_000003.11:g.49064280G= , CM000665.1:g.49064280G= GRCh37
NC_000003.10:g.49039284G= NCBI36
NG_012091.1:g.7596C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2699C= ENSP00000515567.1:p.Ala900=
ENST00000703937.1:c.*1760C= ENSP00000515568.1:n.*1760C=
ENST00000326739.9:c.659C= MANE Select ENSP00000321584.4:p.Ala220=
ENST00000429182.6:c.659C= ENSP00000393525.2:p.Ala220=
ENST00000442157.2:c.584C= ENSP00000403502.2:p.Ala195=
ENST00000462980.2:n.1174C=
ENST00000472328.2:n.725C=
ENST00000491610.2:n.619C=
ENST00000676607.1:n.955C=
ENST00000676627.1:n.1389C=
ENST00000676708.1:n.1939C=
ENST00000676864.1:n.1808C=
ENST00000677010.1:c.695C= ENSP00000503089.1:p.Ala232=
ENST00000677108.1:n.2565C=
ENST00000677168.1:n.1131C=
ENST00000677185.1:n.1222C=
ENST00000677205.1:n.1443C=
ENST00000677344.1:n.1933C=
ENST00000677480.1:c.*336C= ENSP00000504378.1:n.*336C=
ENST00000677519.1:n.1369C=
ENST00000677593.1:n.1215C=
ENST00000677740.1:n.2164C=
ENST00000677991.1:n.1832C=
ENST00000678001.1:n.1152C=
ENST00000678085.1:n.1215C=
ENST00000678177.1:n.2508C=
ENST00000678603.1:n.1737C=
ENST00000678724.1:c.584C= ENSP00000503874.1:p.Ala195=
ENST00000678920.1:n.817C=
ENST00000679019.1:n.1429C=
ENST00000679117.1:c.*474C= ENSP00000503240.1:n.*474C=
ENST00000679339.1:n.1500C=
ENST00000326739.8:c.659C= ENSP00000321584.4:p.Ala220=
ENST00000429182.5:c.453C=
ENST00000442157.1:c.584C= ENSP00000403502.1:p.Ala195=
ENST00000462980.1:n.561C=
ENST00000491610.1:n.619C=
NM_000884.2:c.659C= NP_000875.2:p.Ala220=
XM_006713128.2:c.869C= XP_006713191.1:p.Ala290=
XM_006713128.3:c.869C= XP_006713191.1:p.Ala290=
XM_017006349.1:c.794C= XP_016861838.1:p.Ala265=
XM_017006350.1:c.794C= XP_016861839.1:p.Ala265=
NM_000884.3:c.659C= MANE Select NP_000875.2:p.Ala220=