Canonical Allele Identifier: CA1363291696
Gene: IMPDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026870T= , CM000665.2:g.49026870T= GRCh38
NC_000003.11:g.49064303T= , CM000665.1:g.49064303T= GRCh37
NC_000003.10:g.49039307T= NCBI36
NG_012091.1:g.7573A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2676A= ENSP00000515567.1:p.Val892=
ENST00000703937.1:c.*1737A= ENSP00000515568.1:n.*1737A=
ENST00000326739.9:c.636A= MANE Select ENSP00000321584.4:p.Val212=
ENST00000429182.6:c.636A= ENSP00000393525.2:p.Val212=
ENST00000442157.2:c.561A= ENSP00000403502.2:p.Val187=
ENST00000462980.2:n.1151A=
ENST00000472328.2:n.702A=
ENST00000491610.2:n.596A=
ENST00000676607.1:n.932A=
ENST00000676627.1:n.1366A=
ENST00000676708.1:n.1916A=
ENST00000676864.1:n.1785A=
ENST00000677010.1:c.672A= ENSP00000503089.1:p.Val224=
ENST00000677108.1:n.2542A=
ENST00000677168.1:n.1108A=
ENST00000677185.1:n.1199A=
ENST00000677205.1:n.1420A=
ENST00000677344.1:n.1910A=
ENST00000677480.1:c.*313A= ENSP00000504378.1:n.*313A=
ENST00000677519.1:n.1346A=
ENST00000677593.1:n.1192A=
ENST00000677740.1:n.2141A=
ENST00000677991.1:n.1809A=
ENST00000678001.1:n.1129A=
ENST00000678085.1:n.1192A=
ENST00000678177.1:n.2485A=
ENST00000678603.1:n.1714A=
ENST00000678724.1:c.561A= ENSP00000503874.1:p.Val187=
ENST00000678920.1:n.794A=
ENST00000679019.1:n.1406A=
ENST00000679117.1:c.*451A= ENSP00000503240.1:n.*451A=
ENST00000679339.1:n.1477A=
ENST00000326739.8:c.636A= ENSP00000321584.4:p.Val212=
ENST00000429182.5:c.430A=
ENST00000442157.1:c.561A= ENSP00000403502.1:p.Val187=
ENST00000462980.1:n.538A=
ENST00000491610.1:n.596A=
NM_000884.2:c.636A= NP_000875.2:p.Val212=
XM_006713128.2:c.846A= XP_006713191.1:p.Val282=
XM_006713128.3:c.846A= XP_006713191.1:p.Val282=
XM_017006349.1:c.771A= XP_016861838.1:p.Val257=
XM_017006350.1:c.771A= XP_016861839.1:p.Val257=
NM_000884.3:c.636A= MANE Select NP_000875.2:p.Val212=