Canonical Allele Identifier: CA1363291540

Gene: IMPDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026504A= , CM000665.2:g.49026504A=	GRCh38
NC_000003.11:g.49063937A= , CM000665.1:g.49063937A=	GRCh37
NC_000003.10:g.49038941A=	NCBI36
NG_012091.1:g.7939T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2950+15T=	ENSP00000515567.1:n.2950+15T=
ENST00000703937.1:c.*2011+15T=	ENSP00000515568.1:n.*2011+15T=
ENST00000326739.9:c.910+15T= MANE Select	ENSP00000321584.4:n.910+15T=
ENST00000429182.6:c.910+15T=	ENSP00000393525.2:n.910+15T=
ENST00000442157.2:c.835+15T=	ENSP00000403502.2:n.835+15T=
ENST00000462980.2:n.1425+15T=
ENST00000472328.2:n.976+15T=
ENST00000491610.2:n.885T=
ENST00000676607.1:n.1206+15T=
ENST00000676627.1:n.1640+15T=
ENST00000676708.1:n.2190+15T=
ENST00000676864.1:n.2059+15T=
ENST00000677010.1:c.934+15T=	ENSP00000503089.1:n.934+15T=
ENST00000677108.1:n.2893+15T=
ENST00000677168.1:n.1382+15T=
ENST00000677185.1:n.1473+15T=
ENST00000677205.1:n.1694+15T=
ENST00000677344.1:n.2184+15T=
ENST00000677480.1:c.*587+15T=	ENSP00000504378.1:n.*587+15T=
ENST00000677519.1:n.1620+15T=
ENST00000677593.1:n.1466+15T=
ENST00000677740.1:n.2430T=
ENST00000677991.1:n.2083+15T=
ENST00000678001.1:n.1403+15T=
ENST00000678085.1:n.1543+15T=
ENST00000678177.1:n.2836+15T=
ENST00000678603.1:n.1988+15T=
ENST00000678724.1:c.835+15T=	ENSP00000503874.1:n.835+15T=
ENST00000678920.1:n.1068+15T=
ENST00000679019.1:n.1757+15T=
ENST00000679117.1:c.*725+15T=	ENSP00000503240.1:n.*725+15T=
ENST00000679339.1:n.1751+15T=
ENST00000326739.8:c.910+15T=	ENSP00000321584.4:n.910+15T=
ENST00000429182.5:c.704+15T=
ENST00000462980.1:n.812+15T=
NM_000884.2:c.910+15T=	NP_000875.2:n.910+15T=
XM_006713128.2:c.1120+15T=	XP_006713191.1:n.1120+15T=
XM_006713128.3:c.1120+15T=	XP_006713191.1:n.1120+15T=
XM_017006349.1:c.1045+15T=	XP_016861838.1:n.1045+15T=
XM_017006350.1:c.1045+15T=	XP_016861839.1:n.1045+15T=
NM_000884.3:c.910+15T= MANE Select	NP_000875.2:n.910+15T=