Canonical Allele Identifier: CA1363291663

Gene: IMPDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026770A= , CM000665.2:g.49026770A=	GRCh38
NC_000003.11:g.49064203A= , CM000665.1:g.49064203A=	GRCh37
NC_000003.10:g.49039207A=	NCBI36
NG_012091.1:g.7673T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2776T=	ENSP00000515567.1:p.Cys926=
ENST00000703937.1:c.*1837T=	ENSP00000515568.1:n.*1837T=
ENST00000326739.9:c.736T= MANE Select	ENSP00000321584.4:p.Cys246=
ENST00000429182.6:c.736T=	ENSP00000393525.2:p.Cys246=
ENST00000442157.2:c.661T=	ENSP00000403502.2:p.Cys221=
ENST00000462980.2:n.1251T=
ENST00000472328.2:n.802T=
ENST00000491610.2:n.696T=
ENST00000676607.1:n.1032T=
ENST00000676627.1:n.1466T=
ENST00000676708.1:n.2016T=
ENST00000676864.1:n.1885T=
ENST00000677010.1:c.772T=	ENSP00000503089.1:p.Cys258=
ENST00000677108.1:n.2642T=
ENST00000677168.1:n.1208T=
ENST00000677185.1:n.1299T=
ENST00000677205.1:n.1520T=
ENST00000677344.1:n.2010T=
ENST00000677480.1:c.*413T=	ENSP00000504378.1:n.*413T=
ENST00000677519.1:n.1446T=
ENST00000677593.1:n.1292T=
ENST00000677740.1:n.2241T=
ENST00000677991.1:n.1909T=
ENST00000678001.1:n.1229T=
ENST00000678085.1:n.1292T=
ENST00000678177.1:n.2585T=
ENST00000678603.1:n.1814T=
ENST00000678724.1:c.661T=	ENSP00000503874.1:p.Cys221=
ENST00000678920.1:n.894T=
ENST00000679019.1:n.1506T=
ENST00000679117.1:c.*551T=	ENSP00000503240.1:n.*551T=
ENST00000679339.1:n.1577T=
ENST00000326739.8:c.736T=	ENSP00000321584.4:p.Cys246=
ENST00000429182.5:c.530T=
ENST00000442157.1:c.661T=	ENSP00000403502.1:p.Cys221=
ENST00000462980.1:n.638T=
ENST00000491610.1:n.696T=
NM_000884.2:c.736T=	NP_000875.2:p.Cys246=
XM_006713128.2:c.946T=	XP_006713191.1:p.Cys316=
XM_006713128.3:c.946T=	XP_006713191.1:p.Cys316=
XM_017006349.1:c.871T=	XP_016861838.1:p.Cys291=
XM_017006350.1:c.871T=	XP_016861839.1:p.Cys291=
NM_000884.3:c.736T= MANE Select	NP_000875.2:p.Cys246=