Canonical Allele Identifier: CA352739712
Gene: IMPDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026607G>T , CM000665.2:g.49026607G>T GRCh38
NC_000003.11:g.49064040G>T , CM000665.1:g.49064040G>T GRCh37
NC_000003.10:g.49039044G>T NCBI36
NG_012091.1:g.7836C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2862C>A ENSP00000515567.1:p.Asp954Glu
ENST00000703937.1:c.*1923C>A ENSP00000515568.1:n.*1923C>A
ENST00000326739.9:c.822C>A MANE Select ENSP00000321584.4:p.Asp274Glu
ENST00000429182.6:c.822C>A ENSP00000393525.2:p.Asp274Glu
ENST00000442157.2:c.747C>A ENSP00000403502.2:p.Asp249Glu
ENST00000462980.2:n.1337C>A
ENST00000472328.2:n.888C>A
ENST00000491610.2:n.782C>A
ENST00000676607.1:n.1118C>A
ENST00000676627.1:n.1552C>A
ENST00000676708.1:n.2102C>A
ENST00000676864.1:n.1971C>A
ENST00000677010.1:c.856-10C>A ENSP00000503089.1:n.856-10C>A
ENST00000677108.1:n.2805C>A
ENST00000677168.1:n.1294C>A
ENST00000677185.1:n.1385C>A
ENST00000677205.1:n.1606C>A
ENST00000677344.1:n.2096C>A
ENST00000677480.1:c.*499C>A ENSP00000504378.1:n.*499C>A
ENST00000677519.1:n.1532C>A
ENST00000677593.1:n.1378C>A
ENST00000677740.1:n.2327C>A
ENST00000677991.1:n.1995C>A
ENST00000678001.1:n.1315C>A
ENST00000678085.1:n.1455C>A
ENST00000678177.1:n.2748C>A
ENST00000678603.1:n.1900C>A
ENST00000678724.1:c.747C>A ENSP00000503874.1:p.Asp249Glu
ENST00000678920.1:n.980C>A
ENST00000679019.1:n.1669C>A
ENST00000679117.1:c.*637C>A ENSP00000503240.1:n.*637C>A
ENST00000679339.1:n.1663C>A
ENST00000326739.8:c.822C>A ENSP00000321584.4:p.Asp274Glu
ENST00000429182.5:c.616C>A
ENST00000442157.1:c.747C>A ENSP00000403502.1:p.Asp249Glu
ENST00000462980.1:n.724C>A
ENST00000491610.1:n.782C>A
NM_000884.2:c.822C>A NP_000875.2:p.Asp274Glu
XM_006713128.2:c.1032C>A XP_006713191.1:p.Asp344Glu
XM_006713128.3:c.1032C>A XP_006713191.1:p.Asp344Glu
XM_017006349.1:c.957C>A XP_016861838.1:p.Asp319Glu
XM_017006350.1:c.957C>A XP_016861839.1:p.Asp319Glu
NM_000884.3:c.822C>A MANE Select NP_000875.2:p.Asp274Glu