Canonical Allele Identifier: CA1363291709

Gene: IMPDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026898G= , CM000665.2:g.49026898G=	GRCh38
NC_000003.11:g.49064331G= , CM000665.1:g.49064331G=	GRCh37
NC_000003.10:g.49039335G=	NCBI36
NG_012091.1:g.7545C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2660-12C=	ENSP00000515567.1:n.2660-12C=
ENST00000703937.1:c.*1721-12C=	ENSP00000515568.1:n.*1721-12C=
ENST00000326739.9:c.620-12C= MANE Select	ENSP00000321584.4:n.620-12C=
ENST00000429182.6:c.620-12C=	ENSP00000393525.2:n.620-12C=
ENST00000442157.2:c.545-12C=	ENSP00000403502.2:n.545-12C=
ENST00000462980.2:n.1135-12C=
ENST00000472328.2:n.686-12C=
ENST00000491610.2:n.568C=
ENST00000676607.1:n.916-12C=
ENST00000676627.1:n.1350-12C=
ENST00000676708.1:n.1888C=
ENST00000676864.1:n.1757C=
ENST00000677010.1:c.656-12C=	ENSP00000503089.1:n.656-12C=
ENST00000677108.1:n.2514C=
ENST00000677168.1:n.1092-12C=
ENST00000677185.1:n.1171C=
ENST00000677205.1:n.1392C=
ENST00000677344.1:n.1882C=
ENST00000677480.1:c.*297-12C=	ENSP00000504378.1:n.*297-12C=
ENST00000677519.1:n.1330-12C=
ENST00000677593.1:n.1164C=
ENST00000677740.1:n.2113C=
ENST00000677991.1:n.1793-12C=
ENST00000678001.1:n.1113-12C=
ENST00000678085.1:n.1164C=
ENST00000678177.1:n.2457C=
ENST00000678603.1:n.1698-12C=
ENST00000678724.1:c.545-12C=	ENSP00000503874.1:n.545-12C=
ENST00000678920.1:n.778-12C=
ENST00000679019.1:n.1378C=
ENST00000679117.1:c.*435-12C=	ENSP00000503240.1:n.*435-12C=
ENST00000679339.1:n.1449C=
ENST00000326739.8:c.620-12C=	ENSP00000321584.4:n.620-12C=
ENST00000429182.5:c.414-12C=
ENST00000442157.1:c.545-12C=	ENSP00000403502.1:n.545-12C=
ENST00000462980.1:n.522-12C=
ENST00000491610.1:n.568C=
NM_000884.2:c.620-12C=	NP_000875.2:n.620-12C=
XM_006713128.2:c.830-12C=	XP_006713191.1:n.830-12C=
XM_006713128.3:c.830-12C=	XP_006713191.1:n.830-12C=
XM_017006349.1:c.755-12C=	XP_016861838.1:n.755-12C=
XM_017006350.1:c.755-12C=	XP_016861839.1:n.755-12C=
NM_000884.3:c.620-12C= MANE Select	NP_000875.2:n.620-12C=