Canonical Allele Identifier: CA1363291695

Gene: IMPDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026866C= , CM000665.2:g.49026866C=	GRCh38
NC_000003.11:g.49064299C= , CM000665.1:g.49064299C=	GRCh37
NC_000003.10:g.49039303C=	NCBI36
NG_012091.1:g.7577G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2680G=	ENSP00000515567.1:p.Glu894=
ENST00000703937.1:c.*1741G=	ENSP00000515568.1:n.*1741G=
ENST00000326739.9:c.640G= MANE Select	ENSP00000321584.4:p.Glu214=
ENST00000429182.6:c.640G=	ENSP00000393525.2:p.Glu214=
ENST00000442157.2:c.565G=	ENSP00000403502.2:p.Glu189=
ENST00000462980.2:n.1155G=
ENST00000472328.2:n.706G=
ENST00000491610.2:n.600G=
ENST00000676607.1:n.936G=
ENST00000676627.1:n.1370G=
ENST00000676708.1:n.1920G=
ENST00000676864.1:n.1789G=
ENST00000677010.1:c.676G=	ENSP00000503089.1:p.Glu226=
ENST00000677108.1:n.2546G=
ENST00000677168.1:n.1112G=
ENST00000677185.1:n.1203G=
ENST00000677205.1:n.1424G=
ENST00000677344.1:n.1914G=
ENST00000677480.1:c.*317G=	ENSP00000504378.1:n.*317G=
ENST00000677519.1:n.1350G=
ENST00000677593.1:n.1196G=
ENST00000677740.1:n.2145G=
ENST00000677991.1:n.1813G=
ENST00000678001.1:n.1133G=
ENST00000678085.1:n.1196G=
ENST00000678177.1:n.2489G=
ENST00000678603.1:n.1718G=
ENST00000678724.1:c.565G=	ENSP00000503874.1:p.Glu189=
ENST00000678920.1:n.798G=
ENST00000679019.1:n.1410G=
ENST00000679117.1:c.*455G=	ENSP00000503240.1:n.*455G=
ENST00000679339.1:n.1481G=
ENST00000326739.8:c.640G=	ENSP00000321584.4:p.Glu214=
ENST00000429182.5:c.434G=
ENST00000442157.1:c.565G=	ENSP00000403502.1:p.Glu189=
ENST00000462980.1:n.542G=
ENST00000491610.1:n.600G=
NM_000884.2:c.640G=	NP_000875.2:p.Glu214=
XM_006713128.2:c.850G=	XP_006713191.1:p.Glu284=
XM_006713128.3:c.850G=	XP_006713191.1:p.Glu284=
XM_017006349.1:c.775G=	XP_016861838.1:p.Glu259=
XM_017006350.1:c.775G=	XP_016861839.1:p.Glu259=
NM_000884.3:c.640G= MANE Select	NP_000875.2:p.Glu214=