Canonical Allele Identifier: CA1363291716

Gene: IMPDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026911C= , CM000665.2:g.49026911C=	GRCh38
NC_000003.11:g.49064344C= , CM000665.1:g.49064344C=	GRCh37
NC_000003.10:g.49039348C=	NCBI36
NG_012091.1:g.7532G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2660-25G=	ENSP00000515567.1:n.2660-25G=
ENST00000703937.1:c.*1721-25G=	ENSP00000515568.1:n.*1721-25G=
ENST00000326739.9:c.620-25G= MANE Select	ENSP00000321584.4:n.620-25G=
ENST00000429182.6:c.620-25G=	ENSP00000393525.2:n.620-25G=
ENST00000442157.2:c.545-25G=	ENSP00000403502.2:n.545-25G=
ENST00000462980.2:n.1135-25G=
ENST00000472328.2:n.686-25G=
ENST00000491610.2:n.555G=
ENST00000676607.1:n.916-25G=
ENST00000676627.1:n.1350-25G=
ENST00000676708.1:n.1875G=
ENST00000676864.1:n.1744G=
ENST00000677010.1:c.656-25G=	ENSP00000503089.1:n.656-25G=
ENST00000677108.1:n.2501G=
ENST00000677168.1:n.1092-25G=
ENST00000677185.1:n.1158G=
ENST00000677205.1:n.1379G=
ENST00000677344.1:n.1869G=
ENST00000677480.1:c.*297-25G=	ENSP00000504378.1:n.*297-25G=
ENST00000677519.1:n.1330-25G=
ENST00000677593.1:n.1151G=
ENST00000677740.1:n.2100G=
ENST00000677991.1:n.1793-25G=
ENST00000678001.1:n.1113-25G=
ENST00000678085.1:n.1151G=
ENST00000678177.1:n.2444G=
ENST00000678603.1:n.1698-25G=
ENST00000678724.1:c.545-25G=	ENSP00000503874.1:n.545-25G=
ENST00000678920.1:n.778-25G=
ENST00000679019.1:n.1365G=
ENST00000679117.1:c.*435-25G=	ENSP00000503240.1:n.*435-25G=
ENST00000679339.1:n.1436G=
ENST00000326739.8:c.620-25G=	ENSP00000321584.4:n.620-25G=
ENST00000429182.5:c.414-25G=
ENST00000442157.1:c.545-25G=	ENSP00000403502.1:n.545-25G=
ENST00000462980.1:n.522-25G=
ENST00000491610.1:n.555G=
NM_000884.2:c.620-25G=	NP_000875.2:n.620-25G=
XM_006713128.2:c.830-25G=	XP_006713191.1:n.830-25G=
XM_006713128.3:c.830-25G=	XP_006713191.1:n.830-25G=
XM_017006349.1:c.755-25G=	XP_016861838.1:n.755-25G=
XM_017006350.1:c.755-25G=	XP_016861839.1:n.755-25G=
NM_000884.3:c.620-25G= MANE Select	NP_000875.2:n.620-25G=