Canonical Allele Identifier: CA1363291644

Gene: IMPDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026739T= , CM000665.2:g.49026739T=	GRCh38
NC_000003.11:g.49064172T= , CM000665.1:g.49064172T=	GRCh37
NC_000003.10:g.49039176T=	NCBI36
NG_012091.1:g.7704A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2807A=	ENSP00000515567.1:p.Asp936=
ENST00000703937.1:c.*1868A=	ENSP00000515568.1:n.*1868A=
ENST00000326739.9:c.767A= MANE Select	ENSP00000321584.4:p.Asp256=
ENST00000429182.6:c.767A=	ENSP00000393525.2:p.Asp256=
ENST00000442157.2:c.692A=	ENSP00000403502.2:p.Asp231=
ENST00000462980.2:n.1282A=
ENST00000472328.2:n.833A=
ENST00000491610.2:n.727A=
ENST00000676607.1:n.1063A=
ENST00000676627.1:n.1497A=
ENST00000676708.1:n.2047A=
ENST00000676864.1:n.1916A=
ENST00000677010.1:c.803A=	ENSP00000503089.1:p.Asp268=
ENST00000677108.1:n.2673A=
ENST00000677168.1:n.1239A=
ENST00000677185.1:n.1330A=
ENST00000677205.1:n.1551A=
ENST00000677344.1:n.2041A=
ENST00000677480.1:c.*444A=	ENSP00000504378.1:n.*444A=
ENST00000677519.1:n.1477A=
ENST00000677593.1:n.1323A=
ENST00000677740.1:n.2272A=
ENST00000677991.1:n.1940A=
ENST00000678001.1:n.1260A=
ENST00000678085.1:n.1323A=
ENST00000678177.1:n.2616A=
ENST00000678603.1:n.1845A=
ENST00000678724.1:c.692A=	ENSP00000503874.1:p.Asp231=
ENST00000678920.1:n.925A=
ENST00000679019.1:n.1537A=
ENST00000679117.1:c.*582A=	ENSP00000503240.1:n.*582A=
ENST00000679339.1:n.1608A=
ENST00000326739.8:c.767A=	ENSP00000321584.4:p.Asp256=
ENST00000429182.5:c.561A=
ENST00000442157.1:c.692A=	ENSP00000403502.1:p.Asp231=
ENST00000462980.1:n.669A=
ENST00000491610.1:n.727A=
NM_000884.2:c.767A=	NP_000875.2:p.Asp256=
XM_006713128.2:c.977A=	XP_006713191.1:p.Asp326=
XM_006713128.3:c.977A=	XP_006713191.1:p.Asp326=
XM_017006349.1:c.902A=	XP_016861838.1:p.Asp301=
XM_017006350.1:c.902A=	XP_016861839.1:p.Asp301=
NM_000884.3:c.767A= MANE Select	NP_000875.2:p.Asp256=