Canonical Allele Identifier: CA352740596
Gene: IMPDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026811T>A , CM000665.2:g.49026811T>A GRCh38
NC_000003.11:g.49064244T>A , CM000665.1:g.49064244T>A GRCh37
NC_000003.10:g.49039248T>A NCBI36
NG_012091.1:g.7632A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2735A>T ENSP00000515567.1:p.Asp912Val
ENST00000703937.1:c.*1796A>T ENSP00000515568.1:n.*1796A>T
ENST00000326739.9:c.695A>T MANE Select ENSP00000321584.4:p.Asp232Val
ENST00000429182.6:c.695A>T ENSP00000393525.2:p.Asp232Val
ENST00000442157.2:c.620A>T ENSP00000403502.2:p.Asp207Val
ENST00000462980.2:n.1210A>T
ENST00000472328.2:n.761A>T
ENST00000491610.2:n.655A>T
ENST00000676607.1:n.991A>T
ENST00000676627.1:n.1425A>T
ENST00000676708.1:n.1975A>T
ENST00000676864.1:n.1844A>T
ENST00000677010.1:c.731A>T ENSP00000503089.1:p.Asp244Val
ENST00000677108.1:n.2601A>T
ENST00000677168.1:n.1167A>T
ENST00000677185.1:n.1258A>T
ENST00000677205.1:n.1479A>T
ENST00000677344.1:n.1969A>T
ENST00000677480.1:c.*372A>T ENSP00000504378.1:n.*372A>T
ENST00000677519.1:n.1405A>T
ENST00000677593.1:n.1251A>T
ENST00000677740.1:n.2200A>T
ENST00000677991.1:n.1868A>T
ENST00000678001.1:n.1188A>T
ENST00000678085.1:n.1251A>T
ENST00000678177.1:n.2544A>T
ENST00000678603.1:n.1773A>T
ENST00000678724.1:c.620A>T ENSP00000503874.1:p.Asp207Val
ENST00000678920.1:n.853A>T
ENST00000679019.1:n.1465A>T
ENST00000679117.1:c.*510A>T ENSP00000503240.1:n.*510A>T
ENST00000679339.1:n.1536A>T
ENST00000326739.8:c.695A>T ENSP00000321584.4:p.Asp232Val
ENST00000429182.5:c.489A>T
ENST00000442157.1:c.620A>T ENSP00000403502.1:p.Asp207Val
ENST00000462980.1:n.597A>T
ENST00000491610.1:n.655A>T
NM_000884.2:c.695A>T NP_000875.2:p.Asp232Val
XM_006713128.2:c.905A>T XP_006713191.1:p.Asp302Val
XM_006713128.3:c.905A>T XP_006713191.1:p.Asp302Val
XM_017006349.1:c.830A>T XP_016861838.1:p.Asp277Val
XM_017006350.1:c.830A>T XP_016861839.1:p.Asp277Val
NM_000884.3:c.695A>T MANE Select NP_000875.2:p.Asp232Val