Canonical Allele Identifier: CA1363291647

Gene: IMPDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026743C= , CM000665.2:g.49026743C=	GRCh38
NC_000003.11:g.49064176C= , CM000665.1:g.49064176C=	GRCh37
NC_000003.10:g.49039180C=	NCBI36
NG_012091.1:g.7700G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2803G=	ENSP00000515567.1:p.Asp935=
ENST00000703937.1:c.*1864G=	ENSP00000515568.1:n.*1864G=
ENST00000326739.9:c.763G= MANE Select	ENSP00000321584.4:p.Asp255=
ENST00000429182.6:c.763G=	ENSP00000393525.2:p.Asp255=
ENST00000442157.2:c.688G=	ENSP00000403502.2:p.Asp230=
ENST00000462980.2:n.1278G=
ENST00000472328.2:n.829G=
ENST00000491610.2:n.723G=
ENST00000676607.1:n.1059G=
ENST00000676627.1:n.1493G=
ENST00000676708.1:n.2043G=
ENST00000676864.1:n.1912G=
ENST00000677010.1:c.799G=	ENSP00000503089.1:p.Asp267=
ENST00000677108.1:n.2669G=
ENST00000677168.1:n.1235G=
ENST00000677185.1:n.1326G=
ENST00000677205.1:n.1547G=
ENST00000677344.1:n.2037G=
ENST00000677480.1:c.*440G=	ENSP00000504378.1:n.*440G=
ENST00000677519.1:n.1473G=
ENST00000677593.1:n.1319G=
ENST00000677740.1:n.2268G=
ENST00000677991.1:n.1936G=
ENST00000678001.1:n.1256G=
ENST00000678085.1:n.1319G=
ENST00000678177.1:n.2612G=
ENST00000678603.1:n.1841G=
ENST00000678724.1:c.688G=	ENSP00000503874.1:p.Asp230=
ENST00000678920.1:n.921G=
ENST00000679019.1:n.1533G=
ENST00000679117.1:c.*578G=	ENSP00000503240.1:n.*578G=
ENST00000679339.1:n.1604G=
ENST00000326739.8:c.763G=	ENSP00000321584.4:p.Asp255=
ENST00000429182.5:c.557G=
ENST00000442157.1:c.688G=	ENSP00000403502.1:p.Asp230=
ENST00000462980.1:n.665G=
ENST00000491610.1:n.723G=
NM_000884.2:c.763G=	NP_000875.2:p.Asp255=
XM_006713128.2:c.973G=	XP_006713191.1:p.Asp325=
XM_006713128.3:c.973G=	XP_006713191.1:p.Asp325=
XM_017006349.1:c.898G=	XP_016861838.1:p.Asp300=
XM_017006350.1:c.898G=	XP_016861839.1:p.Asp300=
NM_000884.3:c.763G= MANE Select	NP_000875.2:p.Asp255=