Canonical Allele Identifier: CA1363291759
Gene: IMPDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026991C= , CM000665.2:g.49026991C= GRCh38
NC_000003.11:g.49064424C= , CM000665.1:g.49064424C= GRCh37
NC_000003.10:g.49039428C= NCBI36
NG_012091.1:g.7452G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2628G= ENSP00000515567.1:p.Glu876=
ENST00000703937.1:c.*1689G= ENSP00000515568.1:n.*1689G=
ENST00000326739.9:c.588G= MANE Select ENSP00000321584.4:p.Glu196=
ENST00000429182.6:c.588G= ENSP00000393525.2:p.Glu196=
ENST00000442157.2:c.513G= ENSP00000403502.2:p.Glu171=
ENST00000462980.2:n.1103G=
ENST00000472328.2:n.654G=
ENST00000491610.2:n.475G=
ENST00000676607.1:n.884G=
ENST00000676627.1:n.1318G=
ENST00000676708.1:n.1795G=
ENST00000676864.1:n.1664G=
ENST00000677010.1:c.624G= ENSP00000503089.1:p.Glu208=
ENST00000677108.1:n.2421G=
ENST00000677168.1:n.1060G=
ENST00000677185.1:n.1078G=
ENST00000677205.1:n.1299G=
ENST00000677344.1:n.1789G=
ENST00000677480.1:c.*265G= ENSP00000504378.1:n.*265G=
ENST00000677519.1:n.1298G=
ENST00000677593.1:n.1071G=
ENST00000677740.1:n.2020G=
ENST00000677991.1:n.1761G=
ENST00000678001.1:n.1081G=
ENST00000678085.1:n.1071G=
ENST00000678177.1:n.2364G=
ENST00000678603.1:n.1666G=
ENST00000678724.1:c.513G= ENSP00000503874.1:p.Glu171=
ENST00000678920.1:n.746G=
ENST00000679019.1:n.1285G=
ENST00000679117.1:c.*403G= ENSP00000503240.1:n.*403G=
ENST00000679339.1:n.1356G=
ENST00000326739.8:c.588G= ENSP00000321584.4:p.Glu196=
ENST00000429182.5:c.382G=
ENST00000442157.1:c.513G= ENSP00000403502.1:p.Glu171=
ENST00000462980.1:n.490G=
ENST00000491610.1:n.475G=
NM_000884.2:c.588G= NP_000875.2:p.Glu196=
XM_006713128.2:c.798G= XP_006713191.1:p.Glu266=
XM_006713128.3:c.798G= XP_006713191.1:p.Glu266=
XM_017006349.1:c.723G= XP_016861838.1:p.Glu241=
XM_017006350.1:c.723G= XP_016861839.1:p.Glu241=
NM_000884.3:c.588G= MANE Select NP_000875.2:p.Glu196=