Canonical Allele Identifier: CA352741757

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064425T>A (hg19) ; chr3:g.49026992T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026992T>A , CM000665.2:g.49026992T>A	GRCh38
NC_000003.11:g.49064425T>A , CM000665.1:g.49064425T>A	GRCh37
NC_000003.10:g.49039429T>A	NCBI36
NG_012091.1:g.7451A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2627A>T	ENSP00000515567.1:p.Glu876Val
ENST00000703937.1:c.*1688A>T	ENSP00000515568.1:n.*1688A>T
ENST00000326739.9:c.587A>T MANE Select	ENSP00000321584.4:p.Glu196Val
ENST00000429182.6:c.587A>T	ENSP00000393525.2:p.Glu196Val
ENST00000442157.2:c.512A>T	ENSP00000403502.2:p.Glu171Val
ENST00000462980.2:n.1102A>T
ENST00000472328.2:n.653A>T
ENST00000491610.2:n.474A>T
ENST00000676607.1:n.883A>T
ENST00000676627.1:n.1317A>T
ENST00000676708.1:n.1794A>T
ENST00000676864.1:n.1663A>T
ENST00000677010.1:c.623A>T	ENSP00000503089.1:p.Glu208Val
ENST00000677108.1:n.2420A>T
ENST00000677168.1:n.1059A>T
ENST00000677185.1:n.1077A>T
ENST00000677205.1:n.1298A>T
ENST00000677344.1:n.1788A>T
ENST00000677480.1:c.*264A>T	ENSP00000504378.1:n.*264A>T
ENST00000677519.1:n.1297A>T
ENST00000677593.1:n.1070A>T
ENST00000677740.1:n.2019A>T
ENST00000677991.1:n.1760A>T
ENST00000678001.1:n.1080A>T
ENST00000678085.1:n.1070A>T
ENST00000678177.1:n.2363A>T
ENST00000678603.1:n.1665A>T
ENST00000678724.1:c.512A>T	ENSP00000503874.1:p.Glu171Val
ENST00000678920.1:n.745A>T
ENST00000679019.1:n.1284A>T
ENST00000679117.1:c.*402A>T	ENSP00000503240.1:n.*402A>T
ENST00000679339.1:n.1355A>T
ENST00000326739.8:c.587A>T	ENSP00000321584.4:p.Glu196Val
ENST00000429182.5:c.381A>T
ENST00000442157.1:c.512A>T	ENSP00000403502.1:p.Glu171Val
ENST00000462980.1:n.489A>T
ENST00000491610.1:n.474A>T
NM_000884.2:c.587A>T	NP_000875.2:p.Glu196Val
XM_006713128.2:c.797A>T	XP_006713191.1:p.Glu266Val
XM_006713128.3:c.797A>T	XP_006713191.1:p.Glu266Val
XM_017006349.1:c.722A>T	XP_016861838.1:p.Glu241Val
XM_017006350.1:c.722A>T	XP_016861839.1:p.Glu241Val
NM_000884.3:c.587A>T MANE Select	NP_000875.2:p.Glu196Val