Canonical Allele Identifier: CA1363291674

Gene: IMPDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026810G= , CM000665.2:g.49026810G=	GRCh38
NC_000003.11:g.49064243G= , CM000665.1:g.49064243G=	GRCh37
NC_000003.10:g.49039247G=	NCBI36
NG_012091.1:g.7633C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2736C=	ENSP00000515567.1:p.Asp912=
ENST00000703937.1:c.*1797C=	ENSP00000515568.1:n.*1797C=
ENST00000326739.9:c.696C= MANE Select	ENSP00000321584.4:p.Asp232=
ENST00000429182.6:c.696C=	ENSP00000393525.2:p.Asp232=
ENST00000442157.2:c.621C=	ENSP00000403502.2:p.Asp207=
ENST00000462980.2:n.1211C=
ENST00000472328.2:n.762C=
ENST00000491610.2:n.656C=
ENST00000676607.1:n.992C=
ENST00000676627.1:n.1426C=
ENST00000676708.1:n.1976C=
ENST00000676864.1:n.1845C=
ENST00000677010.1:c.732C=	ENSP00000503089.1:p.Asp244=
ENST00000677108.1:n.2602C=
ENST00000677168.1:n.1168C=
ENST00000677185.1:n.1259C=
ENST00000677205.1:n.1480C=
ENST00000677344.1:n.1970C=
ENST00000677480.1:c.*373C=	ENSP00000504378.1:n.*373C=
ENST00000677519.1:n.1406C=
ENST00000677593.1:n.1252C=
ENST00000677740.1:n.2201C=
ENST00000677991.1:n.1869C=
ENST00000678001.1:n.1189C=
ENST00000678085.1:n.1252C=
ENST00000678177.1:n.2545C=
ENST00000678603.1:n.1774C=
ENST00000678724.1:c.621C=	ENSP00000503874.1:p.Asp207=
ENST00000678920.1:n.854C=
ENST00000679019.1:n.1466C=
ENST00000679117.1:c.*511C=	ENSP00000503240.1:n.*511C=
ENST00000679339.1:n.1537C=
ENST00000326739.8:c.696C=	ENSP00000321584.4:p.Asp232=
ENST00000429182.5:c.490C=
ENST00000442157.1:c.621C=	ENSP00000403502.1:p.Asp207=
ENST00000462980.1:n.598C=
ENST00000491610.1:n.656C=
NM_000884.2:c.696C=	NP_000875.2:p.Asp232=
XM_006713128.2:c.906C=	XP_006713191.1:p.Asp302=
XM_006713128.3:c.906C=	XP_006713191.1:p.Asp302=
XM_017006349.1:c.831C=	XP_016861838.1:p.Asp277=
XM_017006350.1:c.831C=	XP_016861839.1:p.Asp277=
NM_000884.3:c.696C= MANE Select	NP_000875.2:p.Asp232=