Canonical Allele Identifier: CA1363291693

Gene: IMPDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026862T= , CM000665.2:g.49026862T=	GRCh38
NC_000003.11:g.49064295T= , CM000665.1:g.49064295T=	GRCh37
NC_000003.10:g.49039299T=	NCBI36
NG_012091.1:g.7581A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2684A=	ENSP00000515567.1:p.Asp895=
ENST00000703937.1:c.*1745A=	ENSP00000515568.1:n.*1745A=
ENST00000326739.9:c.644A= MANE Select	ENSP00000321584.4:p.Asp215=
ENST00000429182.6:c.644A=	ENSP00000393525.2:p.Asp215=
ENST00000442157.2:c.569A=	ENSP00000403502.2:p.Asp190=
ENST00000462980.2:n.1159A=
ENST00000472328.2:n.710A=
ENST00000491610.2:n.604A=
ENST00000676607.1:n.940A=
ENST00000676627.1:n.1374A=
ENST00000676708.1:n.1924A=
ENST00000676864.1:n.1793A=
ENST00000677010.1:c.680A=	ENSP00000503089.1:p.Asp227=
ENST00000677108.1:n.2550A=
ENST00000677168.1:n.1116A=
ENST00000677185.1:n.1207A=
ENST00000677205.1:n.1428A=
ENST00000677344.1:n.1918A=
ENST00000677480.1:c.*321A=	ENSP00000504378.1:n.*321A=
ENST00000677519.1:n.1354A=
ENST00000677593.1:n.1200A=
ENST00000677740.1:n.2149A=
ENST00000677991.1:n.1817A=
ENST00000678001.1:n.1137A=
ENST00000678085.1:n.1200A=
ENST00000678177.1:n.2493A=
ENST00000678603.1:n.1722A=
ENST00000678724.1:c.569A=	ENSP00000503874.1:p.Asp190=
ENST00000678920.1:n.802A=
ENST00000679019.1:n.1414A=
ENST00000679117.1:c.*459A=	ENSP00000503240.1:n.*459A=
ENST00000679339.1:n.1485A=
ENST00000326739.8:c.644A=	ENSP00000321584.4:p.Asp215=
ENST00000429182.5:c.438A=
ENST00000442157.1:c.569A=	ENSP00000403502.1:p.Asp190=
ENST00000462980.1:n.546A=
ENST00000491610.1:n.604A=
NM_000884.2:c.644A=	NP_000875.2:p.Asp215=
XM_006713128.2:c.854A=	XP_006713191.1:p.Asp285=
XM_006713128.3:c.854A=	XP_006713191.1:p.Asp285=
XM_017006349.1:c.779A=	XP_016861838.1:p.Asp260=
XM_017006350.1:c.779A=	XP_016861839.1:p.Asp260=
NM_000884.3:c.644A= MANE Select	NP_000875.2:p.Asp215=