Canonical Allele Identifier: CA1363291651
Gene: IMPDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026751G= , CM000665.2:g.49026751G= GRCh38
NC_000003.11:g.49064184G= , CM000665.1:g.49064184G= GRCh37
NC_000003.10:g.49039188G= NCBI36
NG_012091.1:g.7692C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2795C= ENSP00000515567.1:p.Thr932=
ENST00000703937.1:c.*1856C= ENSP00000515568.1:n.*1856C=
ENST00000326739.9:c.755C= MANE Select ENSP00000321584.4:p.Thr252=
ENST00000429182.6:c.755C= ENSP00000393525.2:p.Thr252=
ENST00000442157.2:c.680C= ENSP00000403502.2:p.Thr227=
ENST00000462980.2:n.1270C=
ENST00000472328.2:n.821C=
ENST00000491610.2:n.715C=
ENST00000676607.1:n.1051C=
ENST00000676627.1:n.1485C=
ENST00000676708.1:n.2035C=
ENST00000676864.1:n.1904C=
ENST00000677010.1:c.791C= ENSP00000503089.1:p.Thr264=
ENST00000677108.1:n.2661C=
ENST00000677168.1:n.1227C=
ENST00000677185.1:n.1318C=
ENST00000677205.1:n.1539C=
ENST00000677344.1:n.2029C=
ENST00000677480.1:c.*432C= ENSP00000504378.1:n.*432C=
ENST00000677519.1:n.1465C=
ENST00000677593.1:n.1311C=
ENST00000677740.1:n.2260C=
ENST00000677991.1:n.1928C=
ENST00000678001.1:n.1248C=
ENST00000678085.1:n.1311C=
ENST00000678177.1:n.2604C=
ENST00000678603.1:n.1833C=
ENST00000678724.1:c.680C= ENSP00000503874.1:p.Thr227=
ENST00000678920.1:n.913C=
ENST00000679019.1:n.1525C=
ENST00000679117.1:c.*570C= ENSP00000503240.1:n.*570C=
ENST00000679339.1:n.1596C=
ENST00000326739.8:c.755C= ENSP00000321584.4:p.Thr252=
ENST00000429182.5:c.549C=
ENST00000442157.1:c.680C= ENSP00000403502.1:p.Thr227=
ENST00000462980.1:n.657C=
ENST00000491610.1:n.715C=
NM_000884.2:c.755C= NP_000875.2:p.Thr252=
XM_006713128.2:c.965C= XP_006713191.1:p.Thr322=
XM_006713128.3:c.965C= XP_006713191.1:p.Thr322=
XM_017006349.1:c.890C= XP_016861838.1:p.Thr297=
XM_017006350.1:c.890C= XP_016861839.1:p.Thr297=
NM_000884.3:c.755C= MANE Select NP_000875.2:p.Thr252=