Canonical Allele Identifier: CA352740079

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064174A>T (hg19) ; chr3:g.49026741A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026741A>T , CM000665.2:g.49026741A>T	GRCh38
NC_000003.11:g.49064174A>T , CM000665.1:g.49064174A>T	GRCh37
NC_000003.10:g.49039178A>T	NCBI36
NG_012091.1:g.7702T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2805T>A	ENSP00000515567.1:p.Asp935Glu
ENST00000703937.1:c.*1866T>A	ENSP00000515568.1:n.*1866T>A
ENST00000326739.9:c.765T>A MANE Select	ENSP00000321584.4:p.Asp255Glu
ENST00000429182.6:c.765T>A	ENSP00000393525.2:p.Asp255Glu
ENST00000442157.2:c.690T>A	ENSP00000403502.2:p.Asp230Glu
ENST00000462980.2:n.1280T>A
ENST00000472328.2:n.831T>A
ENST00000491610.2:n.725T>A
ENST00000676607.1:n.1061T>A
ENST00000676627.1:n.1495T>A
ENST00000676708.1:n.2045T>A
ENST00000676864.1:n.1914T>A
ENST00000677010.1:c.801T>A	ENSP00000503089.1:p.Asp267Glu
ENST00000677108.1:n.2671T>A
ENST00000677168.1:n.1237T>A
ENST00000677185.1:n.1328T>A
ENST00000677205.1:n.1549T>A
ENST00000677344.1:n.2039T>A
ENST00000677480.1:c.*442T>A	ENSP00000504378.1:n.*442T>A
ENST00000677519.1:n.1475T>A
ENST00000677593.1:n.1321T>A
ENST00000677740.1:n.2270T>A
ENST00000677991.1:n.1938T>A
ENST00000678001.1:n.1258T>A
ENST00000678085.1:n.1321T>A
ENST00000678177.1:n.2614T>A
ENST00000678603.1:n.1843T>A
ENST00000678724.1:c.690T>A	ENSP00000503874.1:p.Asp230Glu
ENST00000678920.1:n.923T>A
ENST00000679019.1:n.1535T>A
ENST00000679117.1:c.*580T>A	ENSP00000503240.1:n.*580T>A
ENST00000679339.1:n.1606T>A
ENST00000326739.8:c.765T>A	ENSP00000321584.4:p.Asp255Glu
ENST00000429182.5:c.559T>A
ENST00000442157.1:c.690T>A	ENSP00000403502.1:p.Asp230Glu
ENST00000462980.1:n.667T>A
ENST00000491610.1:n.725T>A
NM_000884.2:c.765T>A	NP_000875.2:p.Asp255Glu
XM_006713128.2:c.975T>A	XP_006713191.1:p.Asp325Glu
XM_006713128.3:c.975T>A	XP_006713191.1:p.Asp325Glu
XM_017006349.1:c.900T>A	XP_016861838.1:p.Asp300Glu
XM_017006350.1:c.900T>A	XP_016861839.1:p.Asp300Glu
NM_000884.3:c.765T>A MANE Select	NP_000875.2:p.Asp255Glu