Canonical Allele Identifier: CA1363291751
Gene: IMPDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026964C= , CM000665.2:g.49026964C= GRCh38
NC_000003.11:g.49064397C= , CM000665.1:g.49064397C= GRCh37
NC_000003.10:g.49039401C= NCBI36
NG_012091.1:g.7479G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2655G= ENSP00000515567.1:p.Lys885=
ENST00000703937.1:c.*1716G= ENSP00000515568.1:n.*1716G=
ENST00000326739.9:c.615G= MANE Select ENSP00000321584.4:p.Lys205=
ENST00000429182.6:c.615G= ENSP00000393525.2:p.Lys205=
ENST00000442157.2:c.540G= ENSP00000403502.2:p.Lys180=
ENST00000462980.2:n.1130G=
ENST00000472328.2:n.681G=
ENST00000491610.2:n.502G=
ENST00000676607.1:n.911G=
ENST00000676627.1:n.1345G=
ENST00000676708.1:n.1822G=
ENST00000676864.1:n.1691G=
ENST00000677010.1:c.651G= ENSP00000503089.1:p.Lys217=
ENST00000677108.1:n.2448G=
ENST00000677168.1:n.1087G=
ENST00000677185.1:n.1105G=
ENST00000677205.1:n.1326G=
ENST00000677344.1:n.1816G=
ENST00000677480.1:c.*292G= ENSP00000504378.1:n.*292G=
ENST00000677519.1:n.1325G=
ENST00000677593.1:n.1098G=
ENST00000677740.1:n.2047G=
ENST00000677991.1:n.1788G=
ENST00000678001.1:n.1108G=
ENST00000678085.1:n.1098G=
ENST00000678177.1:n.2391G=
ENST00000678603.1:n.1693G=
ENST00000678724.1:c.540G= ENSP00000503874.1:p.Lys180=
ENST00000678920.1:n.773G=
ENST00000679019.1:n.1312G=
ENST00000679117.1:c.*430G= ENSP00000503240.1:n.*430G=
ENST00000679339.1:n.1383G=
ENST00000326739.8:c.615G= ENSP00000321584.4:p.Lys205=
ENST00000429182.5:c.409G=
ENST00000442157.1:c.540G= ENSP00000403502.1:p.Lys180=
ENST00000462980.1:n.517G=
ENST00000491610.1:n.502G=
NM_000884.2:c.615G= NP_000875.2:p.Lys205=
XM_006713128.2:c.825G= XP_006713191.1:p.Lys275=
XM_006713128.3:c.825G= XP_006713191.1:p.Lys275=
XM_017006349.1:c.750G= XP_016861838.1:p.Lys250=
XM_017006350.1:c.750G= XP_016861839.1:p.Lys250=
NM_000884.3:c.615G= MANE Select NP_000875.2:p.Lys205=