Canonical Allele Identifier: CA1363291655
Gene: IMPDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026758T= , CM000665.2:g.49026758T= GRCh38
NC_000003.11:g.49064191T= , CM000665.1:g.49064191T= GRCh37
NC_000003.10:g.49039195T= NCBI36
NG_012091.1:g.7685A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2788A= ENSP00000515567.1:p.Ile930=
ENST00000703937.1:c.*1849A= ENSP00000515568.1:n.*1849A=
ENST00000326739.9:c.748A= MANE Select ENSP00000321584.4:p.Ile250=
ENST00000429182.6:c.748A= ENSP00000393525.2:p.Ile250=
ENST00000442157.2:c.673A= ENSP00000403502.2:p.Ile225=
ENST00000462980.2:n.1263A=
ENST00000472328.2:n.814A=
ENST00000491610.2:n.708A=
ENST00000676607.1:n.1044A=
ENST00000676627.1:n.1478A=
ENST00000676708.1:n.2028A=
ENST00000676864.1:n.1897A=
ENST00000677010.1:c.784A= ENSP00000503089.1:p.Ile262=
ENST00000677108.1:n.2654A=
ENST00000677168.1:n.1220A=
ENST00000677185.1:n.1311A=
ENST00000677205.1:n.1532A=
ENST00000677344.1:n.2022A=
ENST00000677480.1:c.*425A= ENSP00000504378.1:n.*425A=
ENST00000677519.1:n.1458A=
ENST00000677593.1:n.1304A=
ENST00000677740.1:n.2253A=
ENST00000677991.1:n.1921A=
ENST00000678001.1:n.1241A=
ENST00000678085.1:n.1304A=
ENST00000678177.1:n.2597A=
ENST00000678603.1:n.1826A=
ENST00000678724.1:c.673A= ENSP00000503874.1:p.Ile225=
ENST00000678920.1:n.906A=
ENST00000679019.1:n.1518A=
ENST00000679117.1:c.*563A= ENSP00000503240.1:n.*563A=
ENST00000679339.1:n.1589A=
ENST00000326739.8:c.748A= ENSP00000321584.4:p.Ile250=
ENST00000429182.5:c.542A=
ENST00000442157.1:c.673A= ENSP00000403502.1:p.Ile225=
ENST00000462980.1:n.650A=
ENST00000491610.1:n.708A=
NM_000884.2:c.748A= NP_000875.2:p.Ile250=
XM_006713128.2:c.958A= XP_006713191.1:p.Ile320=
XM_006713128.3:c.958A= XP_006713191.1:p.Ile320=
XM_017006349.1:c.883A= XP_016861838.1:p.Ile295=
XM_017006350.1:c.883A= XP_016861839.1:p.Ile295=
NM_000884.3:c.748A= MANE Select NP_000875.2:p.Ile250=