Canonical Allele Identifier: CA1363291756
Gene: IMPDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026974T= , CM000665.2:g.49026974T= GRCh38
NC_000003.11:g.49064407T= , CM000665.1:g.49064407T= GRCh37
NC_000003.10:g.49039411T= NCBI36
NG_012091.1:g.7469A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2645A= ENSP00000515567.1:p.Gln882=
ENST00000703937.1:c.*1706A= ENSP00000515568.1:n.*1706A=
ENST00000326739.9:c.605A= MANE Select ENSP00000321584.4:p.Gln202=
ENST00000429182.6:c.605A= ENSP00000393525.2:p.Gln202=
ENST00000442157.2:c.530A= ENSP00000403502.2:p.Gln177=
ENST00000462980.2:n.1120A=
ENST00000472328.2:n.671A=
ENST00000491610.2:n.492A=
ENST00000676607.1:n.901A=
ENST00000676627.1:n.1335A=
ENST00000676708.1:n.1812A=
ENST00000676864.1:n.1681A=
ENST00000677010.1:c.641A= ENSP00000503089.1:p.Gln214=
ENST00000677108.1:n.2438A=
ENST00000677168.1:n.1077A=
ENST00000677185.1:n.1095A=
ENST00000677205.1:n.1316A=
ENST00000677344.1:n.1806A=
ENST00000677480.1:c.*282A= ENSP00000504378.1:n.*282A=
ENST00000677519.1:n.1315A=
ENST00000677593.1:n.1088A=
ENST00000677740.1:n.2037A=
ENST00000677991.1:n.1778A=
ENST00000678001.1:n.1098A=
ENST00000678085.1:n.1088A=
ENST00000678177.1:n.2381A=
ENST00000678603.1:n.1683A=
ENST00000678724.1:c.530A= ENSP00000503874.1:p.Gln177=
ENST00000678920.1:n.763A=
ENST00000679019.1:n.1302A=
ENST00000679117.1:c.*420A= ENSP00000503240.1:n.*420A=
ENST00000679339.1:n.1373A=
ENST00000326739.8:c.605A= ENSP00000321584.4:p.Gln202=
ENST00000429182.5:c.399A=
ENST00000442157.1:c.530A= ENSP00000403502.1:p.Gln177=
ENST00000462980.1:n.507A=
ENST00000491610.1:n.492A=
NM_000884.2:c.605A= NP_000875.2:p.Gln202=
XM_006713128.2:c.815A= XP_006713191.1:p.Gln272=
XM_006713128.3:c.815A= XP_006713191.1:p.Gln272=
XM_017006349.1:c.740A= XP_016861838.1:p.Gln247=
XM_017006350.1:c.740A= XP_016861839.1:p.Gln247=
NM_000884.3:c.605A= MANE Select NP_000875.2:p.Gln202=