Canonical Allele Identifier: CA1363291666
Gene: IMPDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026780T= , CM000665.2:g.49026780T= GRCh38
NC_000003.11:g.49064213T= , CM000665.1:g.49064213T= GRCh37
NC_000003.10:g.49039217T= NCBI36
NG_012091.1:g.7663A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2766A= ENSP00000515567.1:p.Lys922=
ENST00000703937.1:c.*1827A= ENSP00000515568.1:n.*1827A=
ENST00000326739.9:c.726A= MANE Select ENSP00000321584.4:p.Lys242=
ENST00000429182.6:c.726A= ENSP00000393525.2:p.Lys242=
ENST00000442157.2:c.651A= ENSP00000403502.2:p.Lys217=
ENST00000462980.2:n.1241A=
ENST00000472328.2:n.792A=
ENST00000491610.2:n.686A=
ENST00000676607.1:n.1022A=
ENST00000676627.1:n.1456A=
ENST00000676708.1:n.2006A=
ENST00000676864.1:n.1875A=
ENST00000677010.1:c.762A= ENSP00000503089.1:p.Lys254=
ENST00000677108.1:n.2632A=
ENST00000677168.1:n.1198A=
ENST00000677185.1:n.1289A=
ENST00000677205.1:n.1510A=
ENST00000677344.1:n.2000A=
ENST00000677480.1:c.*403A= ENSP00000504378.1:n.*403A=
ENST00000677519.1:n.1436A=
ENST00000677593.1:n.1282A=
ENST00000677740.1:n.2231A=
ENST00000677991.1:n.1899A=
ENST00000678001.1:n.1219A=
ENST00000678085.1:n.1282A=
ENST00000678177.1:n.2575A=
ENST00000678603.1:n.1804A=
ENST00000678724.1:c.651A= ENSP00000503874.1:p.Lys217=
ENST00000678920.1:n.884A=
ENST00000679019.1:n.1496A=
ENST00000679117.1:c.*541A= ENSP00000503240.1:n.*541A=
ENST00000679339.1:n.1567A=
ENST00000326739.8:c.726A= ENSP00000321584.4:p.Lys242=
ENST00000429182.5:c.520A=
ENST00000442157.1:c.651A= ENSP00000403502.1:p.Lys217=
ENST00000462980.1:n.628A=
ENST00000491610.1:n.686A=
NM_000884.2:c.726A= NP_000875.2:p.Lys242=
XM_006713128.2:c.936A= XP_006713191.1:p.Lys312=
XM_006713128.3:c.936A= XP_006713191.1:p.Lys312=
XM_017006349.1:c.861A= XP_016861838.1:p.Lys287=
XM_017006350.1:c.861A= XP_016861839.1:p.Lys287=
NM_000884.3:c.726A= MANE Select NP_000875.2:p.Lys242=