Canonical Allele Identifier: CA1363291637
Gene: IMPDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026719G= , CM000665.2:g.49026719G= GRCh38
NC_000003.11:g.49064152G= , CM000665.1:g.49064152G= GRCh37
NC_000003.10:g.49039156G= NCBI36
NG_012091.1:g.7724C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2827C= ENSP00000515567.1:p.Leu943=
ENST00000703937.1:c.*1888C= ENSP00000515568.1:n.*1888C=
ENST00000326739.9:c.787C= MANE Select ENSP00000321584.4:p.Leu263=
ENST00000429182.6:c.787C= ENSP00000393525.2:p.Leu263=
ENST00000442157.2:c.712C= ENSP00000403502.2:p.Leu238=
ENST00000462980.2:n.1302C=
ENST00000472328.2:n.853C=
ENST00000491610.2:n.747C=
ENST00000676607.1:n.1083C=
ENST00000676627.1:n.1517C=
ENST00000676708.1:n.2067C=
ENST00000676864.1:n.1936C=
ENST00000677010.1:c.823C= ENSP00000503089.1:p.Leu275=
ENST00000677108.1:n.2693C=
ENST00000677168.1:n.1259C=
ENST00000677185.1:n.1350C=
ENST00000677205.1:n.1571C=
ENST00000677344.1:n.2061C=
ENST00000677480.1:c.*464C= ENSP00000504378.1:n.*464C=
ENST00000677519.1:n.1497C=
ENST00000677593.1:n.1343C=
ENST00000677740.1:n.2292C=
ENST00000677991.1:n.1960C=
ENST00000678001.1:n.1280C=
ENST00000678085.1:n.1343C=
ENST00000678177.1:n.2636C=
ENST00000678603.1:n.1865C=
ENST00000678724.1:c.712C= ENSP00000503874.1:p.Leu238=
ENST00000678920.1:n.945C=
ENST00000679019.1:n.1557C=
ENST00000679117.1:c.*602C= ENSP00000503240.1:n.*602C=
ENST00000679339.1:n.1628C=
ENST00000326739.8:c.787C= ENSP00000321584.4:p.Leu263=
ENST00000429182.5:c.581C=
ENST00000442157.1:c.712C= ENSP00000403502.1:p.Leu238=
ENST00000462980.1:n.689C=
ENST00000491610.1:n.747C=
NM_000884.2:c.787C= NP_000875.2:p.Leu263=
XM_006713128.2:c.997C= XP_006713191.1:p.Leu333=
XM_006713128.3:c.997C= XP_006713191.1:p.Leu333=
XM_017006349.1:c.922C= XP_016861838.1:p.Leu308=
XM_017006350.1:c.922C= XP_016861839.1:p.Leu308=
NM_000884.3:c.787C= MANE Select NP_000875.2:p.Leu263=