Canonical Allele Identifier: CA1363291754
Gene: IMPDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026972G= , CM000665.2:g.49026972G= GRCh38
NC_000003.11:g.49064405G= , CM000665.1:g.49064405G= GRCh37
NC_000003.10:g.49039409G= NCBI36
NG_012091.1:g.7471C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2647C= ENSP00000515567.1:p.Arg883=
ENST00000703937.1:c.*1708C= ENSP00000515568.1:n.*1708C=
ENST00000326739.9:c.607C= MANE Select ENSP00000321584.4:p.Arg203=
ENST00000429182.6:c.607C= ENSP00000393525.2:p.Arg203=
ENST00000442157.2:c.532C= ENSP00000403502.2:p.Arg178=
ENST00000462980.2:n.1122C=
ENST00000472328.2:n.673C=
ENST00000491610.2:n.494C=
ENST00000676607.1:n.903C=
ENST00000676627.1:n.1337C=
ENST00000676708.1:n.1814C=
ENST00000676864.1:n.1683C=
ENST00000677010.1:c.643C= ENSP00000503089.1:p.Arg215=
ENST00000677108.1:n.2440C=
ENST00000677168.1:n.1079C=
ENST00000677185.1:n.1097C=
ENST00000677205.1:n.1318C=
ENST00000677344.1:n.1808C=
ENST00000677480.1:c.*284C= ENSP00000504378.1:n.*284C=
ENST00000677519.1:n.1317C=
ENST00000677593.1:n.1090C=
ENST00000677740.1:n.2039C=
ENST00000677991.1:n.1780C=
ENST00000678001.1:n.1100C=
ENST00000678085.1:n.1090C=
ENST00000678177.1:n.2383C=
ENST00000678603.1:n.1685C=
ENST00000678724.1:c.532C= ENSP00000503874.1:p.Arg178=
ENST00000678920.1:n.765C=
ENST00000679019.1:n.1304C=
ENST00000679117.1:c.*422C= ENSP00000503240.1:n.*422C=
ENST00000679339.1:n.1375C=
ENST00000326739.8:c.607C= ENSP00000321584.4:p.Arg203=
ENST00000429182.5:c.401C=
ENST00000442157.1:c.532C= ENSP00000403502.1:p.Arg178=
ENST00000462980.1:n.509C=
ENST00000491610.1:n.494C=
NM_000884.2:c.607C= NP_000875.2:p.Arg203=
XM_006713128.2:c.817C= XP_006713191.1:p.Arg273=
XM_006713128.3:c.817C= XP_006713191.1:p.Arg273=
XM_017006349.1:c.742C= XP_016861838.1:p.Arg248=
XM_017006350.1:c.742C= XP_016861839.1:p.Arg248=
NM_000884.3:c.607C= MANE Select NP_000875.2:p.Arg203=