Canonical Allele Identifier: CA1363291630

Gene: IMPDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026704C= , CM000665.2:g.49026704C=	GRCh38
NC_000003.11:g.49064137C= , CM000665.1:g.49064137C=	GRCh37
NC_000003.10:g.49039141C=	NCBI36
NG_012091.1:g.7739G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2842G=	ENSP00000515567.1:p.Val948=
ENST00000703937.1:c.*1903G=	ENSP00000515568.1:n.*1903G=
ENST00000326739.9:c.802G= MANE Select	ENSP00000321584.4:p.Val268=
ENST00000429182.6:c.802G=	ENSP00000393525.2:p.Val268=
ENST00000442157.2:c.727G=	ENSP00000403502.2:p.Val243=
ENST00000462980.2:n.1317G=
ENST00000472328.2:n.868G=
ENST00000491610.2:n.762G=
ENST00000676607.1:n.1098G=
ENST00000676627.1:n.1532G=
ENST00000676708.1:n.2082G=
ENST00000676864.1:n.1951G=
ENST00000677010.1:c.838G=	ENSP00000503089.1:p.Val280=
ENST00000677108.1:n.2708G=
ENST00000677168.1:n.1274G=
ENST00000677185.1:n.1365G=
ENST00000677205.1:n.1586G=
ENST00000677344.1:n.2076G=
ENST00000677480.1:c.*479G=	ENSP00000504378.1:n.*479G=
ENST00000677519.1:n.1512G=
ENST00000677593.1:n.1358G=
ENST00000677740.1:n.2307G=
ENST00000677991.1:n.1975G=
ENST00000678001.1:n.1295G=
ENST00000678085.1:n.1358G=
ENST00000678177.1:n.2651G=
ENST00000678603.1:n.1880G=
ENST00000678724.1:c.727G=	ENSP00000503874.1:p.Val243=
ENST00000678920.1:n.960G=
ENST00000679019.1:n.1572G=
ENST00000679117.1:c.*617G=	ENSP00000503240.1:n.*617G=
ENST00000679339.1:n.1643G=
ENST00000326739.8:c.802G=	ENSP00000321584.4:p.Val268=
ENST00000429182.5:c.596G=
ENST00000442157.1:c.727G=	ENSP00000403502.1:p.Val243=
ENST00000462980.1:n.704G=
ENST00000491610.1:n.762G=
NM_000884.2:c.802G=	NP_000875.2:p.Val268=
XM_006713128.2:c.1012G=	XP_006713191.1:p.Val338=
XM_006713128.3:c.1012G=	XP_006713191.1:p.Val338=
XM_017006349.1:c.937G=	XP_016861838.1:p.Val313=
XM_017006350.1:c.937G=	XP_016861839.1:p.Val313=
NM_000884.3:c.802G= MANE Select	NP_000875.2:p.Val268=