Canonical Allele Identifier: CA1363291676
Gene: IMPDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026821T= , CM000665.2:g.49026821T= GRCh38
NC_000003.11:g.49064254T= , CM000665.1:g.49064254T= GRCh37
NC_000003.10:g.49039258T= NCBI36
NG_012091.1:g.7622A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2725A= ENSP00000515567.1:p.Lys909=
ENST00000703937.1:c.*1786A= ENSP00000515568.1:n.*1786A=
ENST00000326739.9:c.685A= MANE Select ENSP00000321584.4:p.Lys229=
ENST00000429182.6:c.685A= ENSP00000393525.2:p.Lys229=
ENST00000442157.2:c.610A= ENSP00000403502.2:p.Lys204=
ENST00000462980.2:n.1200A=
ENST00000472328.2:n.751A=
ENST00000491610.2:n.645A=
ENST00000676607.1:n.981A=
ENST00000676627.1:n.1415A=
ENST00000676708.1:n.1965A=
ENST00000676864.1:n.1834A=
ENST00000677010.1:c.721A= ENSP00000503089.1:p.Lys241=
ENST00000677108.1:n.2591A=
ENST00000677168.1:n.1157A=
ENST00000677185.1:n.1248A=
ENST00000677205.1:n.1469A=
ENST00000677344.1:n.1959A=
ENST00000677480.1:c.*362A= ENSP00000504378.1:n.*362A=
ENST00000677519.1:n.1395A=
ENST00000677593.1:n.1241A=
ENST00000677740.1:n.2190A=
ENST00000677991.1:n.1858A=
ENST00000678001.1:n.1178A=
ENST00000678085.1:n.1241A=
ENST00000678177.1:n.2534A=
ENST00000678603.1:n.1763A=
ENST00000678724.1:c.610A= ENSP00000503874.1:p.Lys204=
ENST00000678920.1:n.843A=
ENST00000679019.1:n.1455A=
ENST00000679117.1:c.*500A= ENSP00000503240.1:n.*500A=
ENST00000679339.1:n.1526A=
ENST00000326739.8:c.685A= ENSP00000321584.4:p.Lys229=
ENST00000429182.5:c.479A=
ENST00000442157.1:c.610A= ENSP00000403502.1:p.Lys204=
ENST00000462980.1:n.587A=
ENST00000491610.1:n.645A=
NM_000884.2:c.685A= NP_000875.2:p.Lys229=
XM_006713128.2:c.895A= XP_006713191.1:p.Lys299=
XM_006713128.3:c.895A= XP_006713191.1:p.Lys299=
XM_017006349.1:c.820A= XP_016861838.1:p.Lys274=
XM_017006350.1:c.820A= XP_016861839.1:p.Lys274=
NM_000884.3:c.685A= MANE Select NP_000875.2:p.Lys229=