Canonical Allele Identifier: CA1363291677
Gene: IMPDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026822C= , CM000665.2:g.49026822C= GRCh38
NC_000003.11:g.49064255C= , CM000665.1:g.49064255C= GRCh37
NC_000003.10:g.49039259C= NCBI36
NG_012091.1:g.7621G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2724G= ENSP00000515567.1:p.Lys908=
ENST00000703937.1:c.*1785G= ENSP00000515568.1:n.*1785G=
ENST00000326739.9:c.684G= MANE Select ENSP00000321584.4:p.Lys228=
ENST00000429182.6:c.684G= ENSP00000393525.2:p.Lys228=
ENST00000442157.2:c.609G= ENSP00000403502.2:p.Lys203=
ENST00000462980.2:n.1199G=
ENST00000472328.2:n.750G=
ENST00000491610.2:n.644G=
ENST00000676607.1:n.980G=
ENST00000676627.1:n.1414G=
ENST00000676708.1:n.1964G=
ENST00000676864.1:n.1833G=
ENST00000677010.1:c.720G= ENSP00000503089.1:p.Lys240=
ENST00000677108.1:n.2590G=
ENST00000677168.1:n.1156G=
ENST00000677185.1:n.1247G=
ENST00000677205.1:n.1468G=
ENST00000677344.1:n.1958G=
ENST00000677480.1:c.*361G= ENSP00000504378.1:n.*361G=
ENST00000677519.1:n.1394G=
ENST00000677593.1:n.1240G=
ENST00000677740.1:n.2189G=
ENST00000677991.1:n.1857G=
ENST00000678001.1:n.1177G=
ENST00000678085.1:n.1240G=
ENST00000678177.1:n.2533G=
ENST00000678603.1:n.1762G=
ENST00000678724.1:c.609G= ENSP00000503874.1:p.Lys203=
ENST00000678920.1:n.842G=
ENST00000679019.1:n.1454G=
ENST00000679117.1:c.*499G= ENSP00000503240.1:n.*499G=
ENST00000679339.1:n.1525G=
ENST00000326739.8:c.684G= ENSP00000321584.4:p.Lys228=
ENST00000429182.5:c.478G=
ENST00000442157.1:c.609G= ENSP00000403502.1:p.Lys203=
ENST00000462980.1:n.586G=
ENST00000491610.1:n.644G=
NM_000884.2:c.684G= NP_000875.2:p.Lys228=
XM_006713128.2:c.894G= XP_006713191.1:p.Lys298=
XM_006713128.3:c.894G= XP_006713191.1:p.Lys298=
XM_017006349.1:c.819G= XP_016861838.1:p.Lys273=
XM_017006350.1:c.819G= XP_016861839.1:p.Lys273=
NM_000884.3:c.684G= MANE Select NP_000875.2:p.Lys228=