Canonical Allele Identifier: CA1363291639

Gene: IMPDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026728G= , CM000665.2:g.49026728G=	GRCh38
NC_000003.11:g.49064161G= , CM000665.1:g.49064161G=	GRCh37
NC_000003.10:g.49039165G=	NCBI36
NG_012091.1:g.7715C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2818C=	ENSP00000515567.1:p.Leu940=
ENST00000703937.1:c.*1879C=	ENSP00000515568.1:n.*1879C=
ENST00000326739.9:c.778C= MANE Select	ENSP00000321584.4:p.Leu260=
ENST00000429182.6:c.778C=	ENSP00000393525.2:p.Leu260=
ENST00000442157.2:c.703C=	ENSP00000403502.2:p.Leu235=
ENST00000462980.2:n.1293C=
ENST00000472328.2:n.844C=
ENST00000491610.2:n.738C=
ENST00000676607.1:n.1074C=
ENST00000676627.1:n.1508C=
ENST00000676708.1:n.2058C=
ENST00000676864.1:n.1927C=
ENST00000677010.1:c.814C=	ENSP00000503089.1:p.Leu272=
ENST00000677108.1:n.2684C=
ENST00000677168.1:n.1250C=
ENST00000677185.1:n.1341C=
ENST00000677205.1:n.1562C=
ENST00000677344.1:n.2052C=
ENST00000677480.1:c.*455C=	ENSP00000504378.1:n.*455C=
ENST00000677519.1:n.1488C=
ENST00000677593.1:n.1334C=
ENST00000677740.1:n.2283C=
ENST00000677991.1:n.1951C=
ENST00000678001.1:n.1271C=
ENST00000678085.1:n.1334C=
ENST00000678177.1:n.2627C=
ENST00000678603.1:n.1856C=
ENST00000678724.1:c.703C=	ENSP00000503874.1:p.Leu235=
ENST00000678920.1:n.936C=
ENST00000679019.1:n.1548C=
ENST00000679117.1:c.*593C=	ENSP00000503240.1:n.*593C=
ENST00000679339.1:n.1619C=
ENST00000326739.8:c.778C=	ENSP00000321584.4:p.Leu260=
ENST00000429182.5:c.572C=
ENST00000442157.1:c.703C=	ENSP00000403502.1:p.Leu235=
ENST00000462980.1:n.680C=
ENST00000491610.1:n.738C=
NM_000884.2:c.778C=	NP_000875.2:p.Leu260=
XM_006713128.2:c.988C=	XP_006713191.1:p.Leu330=
XM_006713128.3:c.988C=	XP_006713191.1:p.Leu330=
XM_017006349.1:c.913C=	XP_016861838.1:p.Leu305=
XM_017006350.1:c.913C=	XP_016861839.1:p.Leu305=
NM_000884.3:c.778C= MANE Select	NP_000875.2:p.Leu260=