Canonical Allele Identifier: CA1363291667
Gene: IMPDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026786G= , CM000665.2:g.49026786G= GRCh38
NC_000003.11:g.49064219G= , CM000665.1:g.49064219G= GRCh37
NC_000003.10:g.49039223G= NCBI36
NG_012091.1:g.7657C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2760C= ENSP00000515567.1:p.Ala920=
ENST00000703937.1:c.*1821C= ENSP00000515568.1:n.*1821C=
ENST00000326739.9:c.720C= MANE Select ENSP00000321584.4:p.Ala240=
ENST00000429182.6:c.720C= ENSP00000393525.2:p.Ala240=
ENST00000442157.2:c.645C= ENSP00000403502.2:p.Ala215=
ENST00000462980.2:n.1235C=
ENST00000472328.2:n.786C=
ENST00000491610.2:n.680C=
ENST00000676607.1:n.1016C=
ENST00000676627.1:n.1450C=
ENST00000676708.1:n.2000C=
ENST00000676864.1:n.1869C=
ENST00000677010.1:c.756C= ENSP00000503089.1:p.Ala252=
ENST00000677108.1:n.2626C=
ENST00000677168.1:n.1192C=
ENST00000677185.1:n.1283C=
ENST00000677205.1:n.1504C=
ENST00000677344.1:n.1994C=
ENST00000677480.1:c.*397C= ENSP00000504378.1:n.*397C=
ENST00000677519.1:n.1430C=
ENST00000677593.1:n.1276C=
ENST00000677740.1:n.2225C=
ENST00000677991.1:n.1893C=
ENST00000678001.1:n.1213C=
ENST00000678085.1:n.1276C=
ENST00000678177.1:n.2569C=
ENST00000678603.1:n.1798C=
ENST00000678724.1:c.645C= ENSP00000503874.1:p.Ala215=
ENST00000678920.1:n.878C=
ENST00000679019.1:n.1490C=
ENST00000679117.1:c.*535C= ENSP00000503240.1:n.*535C=
ENST00000679339.1:n.1561C=
ENST00000326739.8:c.720C= ENSP00000321584.4:p.Ala240=
ENST00000429182.5:c.514C=
ENST00000442157.1:c.645C= ENSP00000403502.1:p.Ala215=
ENST00000462980.1:n.622C=
ENST00000491610.1:n.680C=
NM_000884.2:c.720C= NP_000875.2:p.Ala240=
XM_006713128.2:c.930C= XP_006713191.1:p.Ala310=
XM_006713128.3:c.930C= XP_006713191.1:p.Ala310=
XM_017006349.1:c.855C= XP_016861838.1:p.Ala285=
XM_017006350.1:c.855C= XP_016861839.1:p.Ala285=
NM_000884.3:c.720C= MANE Select NP_000875.2:p.Ala240=