Canonical Allele Identifier: CA1363291678
Gene: IMPDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026832G= , CM000665.2:g.49026832G= GRCh38
NC_000003.11:g.49064265G= , CM000665.1:g.49064265G= GRCh37
NC_000003.10:g.49039269G= NCBI36
NG_012091.1:g.7611C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2714C= ENSP00000515567.1:p.Thr905=
ENST00000703937.1:c.*1775C= ENSP00000515568.1:n.*1775C=
ENST00000326739.9:c.674C= MANE Select ENSP00000321584.4:p.Thr225=
ENST00000429182.6:c.674C= ENSP00000393525.2:p.Thr225=
ENST00000442157.2:c.599C= ENSP00000403502.2:p.Thr200=
ENST00000462980.2:n.1189C=
ENST00000472328.2:n.740C=
ENST00000491610.2:n.634C=
ENST00000676607.1:n.970C=
ENST00000676627.1:n.1404C=
ENST00000676708.1:n.1954C=
ENST00000676864.1:n.1823C=
ENST00000677010.1:c.710C= ENSP00000503089.1:p.Thr237=
ENST00000677108.1:n.2580C=
ENST00000677168.1:n.1146C=
ENST00000677185.1:n.1237C=
ENST00000677205.1:n.1458C=
ENST00000677344.1:n.1948C=
ENST00000677480.1:c.*351C= ENSP00000504378.1:n.*351C=
ENST00000677519.1:n.1384C=
ENST00000677593.1:n.1230C=
ENST00000677740.1:n.2179C=
ENST00000677991.1:n.1847C=
ENST00000678001.1:n.1167C=
ENST00000678085.1:n.1230C=
ENST00000678177.1:n.2523C=
ENST00000678603.1:n.1752C=
ENST00000678724.1:c.599C= ENSP00000503874.1:p.Thr200=
ENST00000678920.1:n.832C=
ENST00000679019.1:n.1444C=
ENST00000679117.1:c.*489C= ENSP00000503240.1:n.*489C=
ENST00000679339.1:n.1515C=
ENST00000326739.8:c.674C= ENSP00000321584.4:p.Thr225=
ENST00000429182.5:c.468C=
ENST00000442157.1:c.599C= ENSP00000403502.1:p.Thr200=
ENST00000462980.1:n.576C=
ENST00000491610.1:n.634C=
NM_000884.2:c.674C= NP_000875.2:p.Thr225=
XM_006713128.2:c.884C= XP_006713191.1:p.Thr295=
XM_006713128.3:c.884C= XP_006713191.1:p.Thr295=
XM_017006349.1:c.809C= XP_016861838.1:p.Thr270=
XM_017006350.1:c.809C= XP_016861839.1:p.Thr270=
NM_000884.3:c.674C= MANE Select NP_000875.2:p.Thr225=