Canonical Allele Identifier: CA1363291661
Gene: IMPDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026768A= , CM000665.2:g.49026768A= GRCh38
NC_000003.11:g.49064201A= , CM000665.1:g.49064201A= GRCh37
NC_000003.10:g.49039205A= NCBI36
NG_012091.1:g.7675T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2778T= ENSP00000515567.1:p.Cys926=
ENST00000703937.1:c.*1839T= ENSP00000515568.1:n.*1839T=
ENST00000326739.9:c.738T= MANE Select ENSP00000321584.4:p.Cys246=
ENST00000429182.6:c.738T= ENSP00000393525.2:p.Cys246=
ENST00000442157.2:c.663T= ENSP00000403502.2:p.Cys221=
ENST00000462980.2:n.1253T=
ENST00000472328.2:n.804T=
ENST00000491610.2:n.698T=
ENST00000676607.1:n.1034T=
ENST00000676627.1:n.1468T=
ENST00000676708.1:n.2018T=
ENST00000676864.1:n.1887T=
ENST00000677010.1:c.774T= ENSP00000503089.1:p.Cys258=
ENST00000677108.1:n.2644T=
ENST00000677168.1:n.1210T=
ENST00000677185.1:n.1301T=
ENST00000677205.1:n.1522T=
ENST00000677344.1:n.2012T=
ENST00000677480.1:c.*415T= ENSP00000504378.1:n.*415T=
ENST00000677519.1:n.1448T=
ENST00000677593.1:n.1294T=
ENST00000677740.1:n.2243T=
ENST00000677991.1:n.1911T=
ENST00000678001.1:n.1231T=
ENST00000678085.1:n.1294T=
ENST00000678177.1:n.2587T=
ENST00000678603.1:n.1816T=
ENST00000678724.1:c.663T= ENSP00000503874.1:p.Cys221=
ENST00000678920.1:n.896T=
ENST00000679019.1:n.1508T=
ENST00000679117.1:c.*553T= ENSP00000503240.1:n.*553T=
ENST00000679339.1:n.1579T=
ENST00000326739.8:c.738T= ENSP00000321584.4:p.Cys246=
ENST00000429182.5:c.532T=
ENST00000442157.1:c.663T= ENSP00000403502.1:p.Cys221=
ENST00000462980.1:n.640T=
ENST00000491610.1:n.698T=
NM_000884.2:c.738T= NP_000875.2:p.Cys246=
XM_006713128.2:c.948T= XP_006713191.1:p.Cys316=
XM_006713128.3:c.948T= XP_006713191.1:p.Cys316=
XM_017006349.1:c.873T= XP_016861838.1:p.Cys291=
XM_017006350.1:c.873T= XP_016861839.1:p.Cys291=
NM_000884.3:c.738T= MANE Select NP_000875.2:p.Cys246=