Canonical Allele Identifier: CA1363291683

Gene: IMPDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026839C= , CM000665.2:g.49026839C=	GRCh38
NC_000003.11:g.49064272C= , CM000665.1:g.49064272C=	GRCh37
NC_000003.10:g.49039276C=	NCBI36
NG_012091.1:g.7604G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2707G=	ENSP00000515567.1:p.Ala903=
ENST00000703937.1:c.*1768G=	ENSP00000515568.1:n.*1768G=
ENST00000326739.9:c.667G= MANE Select	ENSP00000321584.4:p.Ala223=
ENST00000429182.6:c.667G=	ENSP00000393525.2:p.Ala223=
ENST00000442157.2:c.592G=	ENSP00000403502.2:p.Ala198=
ENST00000462980.2:n.1182G=
ENST00000472328.2:n.733G=
ENST00000491610.2:n.627G=
ENST00000676607.1:n.963G=
ENST00000676627.1:n.1397G=
ENST00000676708.1:n.1947G=
ENST00000676864.1:n.1816G=
ENST00000677010.1:c.703G=	ENSP00000503089.1:p.Ala235=
ENST00000677108.1:n.2573G=
ENST00000677168.1:n.1139G=
ENST00000677185.1:n.1230G=
ENST00000677205.1:n.1451G=
ENST00000677344.1:n.1941G=
ENST00000677480.1:c.*344G=	ENSP00000504378.1:n.*344G=
ENST00000677519.1:n.1377G=
ENST00000677593.1:n.1223G=
ENST00000677740.1:n.2172G=
ENST00000677991.1:n.1840G=
ENST00000678001.1:n.1160G=
ENST00000678085.1:n.1223G=
ENST00000678177.1:n.2516G=
ENST00000678603.1:n.1745G=
ENST00000678724.1:c.592G=	ENSP00000503874.1:p.Ala198=
ENST00000678920.1:n.825G=
ENST00000679019.1:n.1437G=
ENST00000679117.1:c.*482G=	ENSP00000503240.1:n.*482G=
ENST00000679339.1:n.1508G=
ENST00000326739.8:c.667G=	ENSP00000321584.4:p.Ala223=
ENST00000429182.5:c.461G=
ENST00000442157.1:c.592G=	ENSP00000403502.1:p.Ala198=
ENST00000462980.1:n.569G=
ENST00000491610.1:n.627G=
NM_000884.2:c.667G=	NP_000875.2:p.Ala223=
XM_006713128.2:c.877G=	XP_006713191.1:p.Ala293=
XM_006713128.3:c.877G=	XP_006713191.1:p.Ala293=
XM_017006349.1:c.802G=	XP_016861838.1:p.Ala268=
XM_017006350.1:c.802G=	XP_016861839.1:p.Ala268=
NM_000884.3:c.667G= MANE Select	NP_000875.2:p.Ala223=