Canonical Allele Identifier: CA1363291752
Gene: IMPDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026965T= , CM000665.2:g.49026965T= GRCh38
NC_000003.11:g.49064398T= , CM000665.1:g.49064398T= GRCh37
NC_000003.10:g.49039402T= NCBI36
NG_012091.1:g.7478A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2654A= ENSP00000515567.1:p.Lys885=
ENST00000703937.1:c.*1715A= ENSP00000515568.1:n.*1715A=
ENST00000326739.9:c.614A= MANE Select ENSP00000321584.4:p.Lys205=
ENST00000429182.6:c.614A= ENSP00000393525.2:p.Lys205=
ENST00000442157.2:c.539A= ENSP00000403502.2:p.Lys180=
ENST00000462980.2:n.1129A=
ENST00000472328.2:n.680A=
ENST00000491610.2:n.501A=
ENST00000676607.1:n.910A=
ENST00000676627.1:n.1344A=
ENST00000676708.1:n.1821A=
ENST00000676864.1:n.1690A=
ENST00000677010.1:c.650A= ENSP00000503089.1:p.Lys217=
ENST00000677108.1:n.2447A=
ENST00000677168.1:n.1086A=
ENST00000677185.1:n.1104A=
ENST00000677205.1:n.1325A=
ENST00000677344.1:n.1815A=
ENST00000677480.1:c.*291A= ENSP00000504378.1:n.*291A=
ENST00000677519.1:n.1324A=
ENST00000677593.1:n.1097A=
ENST00000677740.1:n.2046A=
ENST00000677991.1:n.1787A=
ENST00000678001.1:n.1107A=
ENST00000678085.1:n.1097A=
ENST00000678177.1:n.2390A=
ENST00000678603.1:n.1692A=
ENST00000678724.1:c.539A= ENSP00000503874.1:p.Lys180=
ENST00000678920.1:n.772A=
ENST00000679019.1:n.1311A=
ENST00000679117.1:c.*429A= ENSP00000503240.1:n.*429A=
ENST00000679339.1:n.1382A=
ENST00000326739.8:c.614A= ENSP00000321584.4:p.Lys205=
ENST00000429182.5:c.408A=
ENST00000442157.1:c.539A= ENSP00000403502.1:p.Lys180=
ENST00000462980.1:n.516A=
ENST00000491610.1:n.501A=
NM_000884.2:c.614A= NP_000875.2:p.Lys205=
XM_006713128.2:c.824A= XP_006713191.1:p.Lys275=
XM_006713128.3:c.824A= XP_006713191.1:p.Lys275=
XM_017006349.1:c.749A= XP_016861838.1:p.Lys250=
XM_017006350.1:c.749A= XP_016861839.1:p.Lys250=
NM_000884.3:c.614A= MANE Select NP_000875.2:p.Lys205=