Canonical Allele Identifier: CA1363291584

Gene: IMPDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026614G= , CM000665.2:g.49026614G=	GRCh38
NC_000003.11:g.49064047G= , CM000665.1:g.49064047G=	GRCh37
NC_000003.10:g.49039051G=	NCBI36
NG_012091.1:g.7829C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2860-5C=	ENSP00000515567.1:n.2860-5C=
ENST00000703937.1:c.*1921-5C=	ENSP00000515568.1:n.*1921-5C=
ENST00000326739.9:c.820-5C= MANE Select	ENSP00000321584.4:n.820-5C=
ENST00000429182.6:c.820-5C=	ENSP00000393525.2:n.820-5C=
ENST00000442157.2:c.745-5C=	ENSP00000403502.2:n.745-5C=
ENST00000462980.2:n.1335-5C=
ENST00000472328.2:n.886-5C=
ENST00000491610.2:n.780-5C=
ENST00000676607.1:n.1116-5C=
ENST00000676627.1:n.1550-5C=
ENST00000676708.1:n.2100-5C=
ENST00000676864.1:n.1969-5C=
ENST00000677010.1:c.856-17C=	ENSP00000503089.1:n.856-17C=
ENST00000677108.1:n.2798C=
ENST00000677168.1:n.1292-5C=
ENST00000677185.1:n.1383-5C=
ENST00000677205.1:n.1604-5C=
ENST00000677344.1:n.2094-5C=
ENST00000677480.1:c.*497-5C=	ENSP00000504378.1:n.*497-5C=
ENST00000677519.1:n.1530-5C=
ENST00000677593.1:n.1376-5C=
ENST00000677740.1:n.2325-5C=
ENST00000677991.1:n.1993-5C=
ENST00000678001.1:n.1313-5C=
ENST00000678085.1:n.1448C=
ENST00000678177.1:n.2741C=
ENST00000678603.1:n.1898-5C=
ENST00000678724.1:c.745-5C=	ENSP00000503874.1:n.745-5C=
ENST00000678920.1:n.978-5C=
ENST00000679019.1:n.1662C=
ENST00000679117.1:c.*635-5C=	ENSP00000503240.1:n.*635-5C=
ENST00000679339.1:n.1661-5C=
ENST00000326739.8:c.820-5C=	ENSP00000321584.4:n.820-5C=
ENST00000429182.5:c.614-5C=
ENST00000442157.1:c.745-5C=	ENSP00000403502.1:n.745-5C=
ENST00000462980.1:n.722-5C=
ENST00000491610.1:n.780-5C=
NM_000884.2:c.820-5C=	NP_000875.2:n.820-5C=
XM_006713128.2:c.1030-5C=	XP_006713191.1:n.1030-5C=
XM_006713128.3:c.1030-5C=	XP_006713191.1:n.1030-5C=
XM_017006349.1:c.955-5C=	XP_016861838.1:n.955-5C=
XM_017006350.1:c.955-5C=	XP_016861839.1:n.955-5C=
NM_000884.3:c.820-5C= MANE Select	NP_000875.2:n.820-5C=