Canonical Allele Identifier: CA352740432
Gene: IMPDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026785T>C , CM000665.2:g.49026785T>C GRCh38
NC_000003.11:g.49064218T>C , CM000665.1:g.49064218T>C GRCh37
NC_000003.10:g.49039222T>C NCBI36
NG_012091.1:g.7658A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2761A>G ENSP00000515567.1:p.Lys921Glu
ENST00000703937.1:c.*1822A>G ENSP00000515568.1:n.*1822A>G
ENST00000326739.9:c.721A>G MANE Select ENSP00000321584.4:p.Lys241Glu
ENST00000429182.6:c.721A>G ENSP00000393525.2:p.Lys241Glu
ENST00000442157.2:c.646A>G ENSP00000403502.2:p.Lys216Glu
ENST00000462980.2:n.1236A>G
ENST00000472328.2:n.787A>G
ENST00000491610.2:n.681A>G
ENST00000676607.1:n.1017A>G
ENST00000676627.1:n.1451A>G
ENST00000676708.1:n.2001A>G
ENST00000676864.1:n.1870A>G
ENST00000677010.1:c.757A>G ENSP00000503089.1:p.Lys253Glu
ENST00000677108.1:n.2627A>G
ENST00000677168.1:n.1193A>G
ENST00000677185.1:n.1284A>G
ENST00000677205.1:n.1505A>G
ENST00000677344.1:n.1995A>G
ENST00000677480.1:c.*398A>G ENSP00000504378.1:n.*398A>G
ENST00000677519.1:n.1431A>G
ENST00000677593.1:n.1277A>G
ENST00000677740.1:n.2226A>G
ENST00000677991.1:n.1894A>G
ENST00000678001.1:n.1214A>G
ENST00000678085.1:n.1277A>G
ENST00000678177.1:n.2570A>G
ENST00000678603.1:n.1799A>G
ENST00000678724.1:c.646A>G ENSP00000503874.1:p.Lys216Glu
ENST00000678920.1:n.879A>G
ENST00000679019.1:n.1491A>G
ENST00000679117.1:c.*536A>G ENSP00000503240.1:n.*536A>G
ENST00000679339.1:n.1562A>G
ENST00000326739.8:c.721A>G ENSP00000321584.4:p.Lys241Glu
ENST00000429182.5:c.515A>G
ENST00000442157.1:c.646A>G ENSP00000403502.1:p.Lys216Glu
ENST00000462980.1:n.623A>G
ENST00000491610.1:n.681A>G
NM_000884.2:c.721A>G NP_000875.2:p.Lys241Glu
XM_006713128.2:c.931A>G XP_006713191.1:p.Lys311Glu
XM_006713128.3:c.931A>G XP_006713191.1:p.Lys311Glu
XM_017006349.1:c.856A>G XP_016861838.1:p.Lys286Glu
XM_017006350.1:c.856A>G XP_016861839.1:p.Lys286Glu
NM_000884.3:c.721A>G MANE Select NP_000875.2:p.Lys241Glu