Canonical Allele Identifier: CA352740085

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064175T>A (hg19) ; chr3:g.49026742T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026742T>A , CM000665.2:g.49026742T>A	GRCh38
NC_000003.11:g.49064175T>A , CM000665.1:g.49064175T>A	GRCh37
NC_000003.10:g.49039179T>A	NCBI36
NG_012091.1:g.7701A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2804A>T	ENSP00000515567.1:p.Asp935Val
ENST00000703937.1:c.*1865A>T	ENSP00000515568.1:n.*1865A>T
ENST00000326739.9:c.764A>T MANE Select	ENSP00000321584.4:p.Asp255Val
ENST00000429182.6:c.764A>T	ENSP00000393525.2:p.Asp255Val
ENST00000442157.2:c.689A>T	ENSP00000403502.2:p.Asp230Val
ENST00000462980.2:n.1279A>T
ENST00000472328.2:n.830A>T
ENST00000491610.2:n.724A>T
ENST00000676607.1:n.1060A>T
ENST00000676627.1:n.1494A>T
ENST00000676708.1:n.2044A>T
ENST00000676864.1:n.1913A>T
ENST00000677010.1:c.800A>T	ENSP00000503089.1:p.Asp267Val
ENST00000677108.1:n.2670A>T
ENST00000677168.1:n.1236A>T
ENST00000677185.1:n.1327A>T
ENST00000677205.1:n.1548A>T
ENST00000677344.1:n.2038A>T
ENST00000677480.1:c.*441A>T	ENSP00000504378.1:n.*441A>T
ENST00000677519.1:n.1474A>T
ENST00000677593.1:n.1320A>T
ENST00000677740.1:n.2269A>T
ENST00000677991.1:n.1937A>T
ENST00000678001.1:n.1257A>T
ENST00000678085.1:n.1320A>T
ENST00000678177.1:n.2613A>T
ENST00000678603.1:n.1842A>T
ENST00000678724.1:c.689A>T	ENSP00000503874.1:p.Asp230Val
ENST00000678920.1:n.922A>T
ENST00000679019.1:n.1534A>T
ENST00000679117.1:c.*579A>T	ENSP00000503240.1:n.*579A>T
ENST00000679339.1:n.1605A>T
ENST00000326739.8:c.764A>T	ENSP00000321584.4:p.Asp255Val
ENST00000429182.5:c.558A>T
ENST00000442157.1:c.689A>T	ENSP00000403502.1:p.Asp230Val
ENST00000462980.1:n.666A>T
ENST00000491610.1:n.724A>T
NM_000884.2:c.764A>T	NP_000875.2:p.Asp255Val
XM_006713128.2:c.974A>T	XP_006713191.1:p.Asp325Val
XM_006713128.3:c.974A>T	XP_006713191.1:p.Asp325Val
XM_017006349.1:c.899A>T	XP_016861838.1:p.Asp300Val
XM_017006350.1:c.899A>T	XP_016861839.1:p.Asp300Val
NM_000884.3:c.764A>T MANE Select	NP_000875.2:p.Asp255Val