Canonical Allele Identifier: CA1363291649

Gene: IMPDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026747A= , CM000665.2:g.49026747A=	GRCh38
NC_000003.11:g.49064180A= , CM000665.1:g.49064180A=	GRCh37
NC_000003.10:g.49039184A=	NCBI36
NG_012091.1:g.7696T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2799T=	ENSP00000515567.1:p.His933=
ENST00000703937.1:c.*1860T=	ENSP00000515568.1:n.*1860T=
ENST00000326739.9:c.759T= MANE Select	ENSP00000321584.4:p.His253=
ENST00000429182.6:c.759T=	ENSP00000393525.2:p.His253=
ENST00000442157.2:c.684T=	ENSP00000403502.2:p.His228=
ENST00000462980.2:n.1274T=
ENST00000472328.2:n.825T=
ENST00000491610.2:n.719T=
ENST00000676607.1:n.1055T=
ENST00000676627.1:n.1489T=
ENST00000676708.1:n.2039T=
ENST00000676864.1:n.1908T=
ENST00000677010.1:c.795T=	ENSP00000503089.1:p.His265=
ENST00000677108.1:n.2665T=
ENST00000677168.1:n.1231T=
ENST00000677185.1:n.1322T=
ENST00000677205.1:n.1543T=
ENST00000677344.1:n.2033T=
ENST00000677480.1:c.*436T=	ENSP00000504378.1:n.*436T=
ENST00000677519.1:n.1469T=
ENST00000677593.1:n.1315T=
ENST00000677740.1:n.2264T=
ENST00000677991.1:n.1932T=
ENST00000678001.1:n.1252T=
ENST00000678085.1:n.1315T=
ENST00000678177.1:n.2608T=
ENST00000678603.1:n.1837T=
ENST00000678724.1:c.684T=	ENSP00000503874.1:p.His228=
ENST00000678920.1:n.917T=
ENST00000679019.1:n.1529T=
ENST00000679117.1:c.*574T=	ENSP00000503240.1:n.*574T=
ENST00000679339.1:n.1600T=
ENST00000326739.8:c.759T=	ENSP00000321584.4:p.His253=
ENST00000429182.5:c.553T=
ENST00000442157.1:c.684T=	ENSP00000403502.1:p.His228=
ENST00000462980.1:n.661T=
ENST00000491610.1:n.719T=
NM_000884.2:c.759T=	NP_000875.2:p.His253=
XM_006713128.2:c.969T=	XP_006713191.1:p.His323=
XM_006713128.3:c.969T=	XP_006713191.1:p.His323=
XM_017006349.1:c.894T=	XP_016861838.1:p.His298=
XM_017006350.1:c.894T=	XP_016861839.1:p.His298=
NM_000884.3:c.759T= MANE Select	NP_000875.2:p.His253=