Canonical Allele Identifier: CA352740071

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064172T>A (hg19) ; chr3:g.49026739T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026739T>A , CM000665.2:g.49026739T>A	GRCh38
NC_000003.11:g.49064172T>A , CM000665.1:g.49064172T>A	GRCh37
NC_000003.10:g.49039176T>A	NCBI36
NG_012091.1:g.7704A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2807A>T	ENSP00000515567.1:p.Asp936Val
ENST00000703937.1:c.*1868A>T	ENSP00000515568.1:n.*1868A>T
ENST00000326739.9:c.767A>T MANE Select	ENSP00000321584.4:p.Asp256Val
ENST00000429182.6:c.767A>T	ENSP00000393525.2:p.Asp256Val
ENST00000442157.2:c.692A>T	ENSP00000403502.2:p.Asp231Val
ENST00000462980.2:n.1282A>T
ENST00000472328.2:n.833A>T
ENST00000491610.2:n.727A>T
ENST00000676607.1:n.1063A>T
ENST00000676627.1:n.1497A>T
ENST00000676708.1:n.2047A>T
ENST00000676864.1:n.1916A>T
ENST00000677010.1:c.803A>T	ENSP00000503089.1:p.Asp268Val
ENST00000677108.1:n.2673A>T
ENST00000677168.1:n.1239A>T
ENST00000677185.1:n.1330A>T
ENST00000677205.1:n.1551A>T
ENST00000677344.1:n.2041A>T
ENST00000677480.1:c.*444A>T	ENSP00000504378.1:n.*444A>T
ENST00000677519.1:n.1477A>T
ENST00000677593.1:n.1323A>T
ENST00000677740.1:n.2272A>T
ENST00000677991.1:n.1940A>T
ENST00000678001.1:n.1260A>T
ENST00000678085.1:n.1323A>T
ENST00000678177.1:n.2616A>T
ENST00000678603.1:n.1845A>T
ENST00000678724.1:c.692A>T	ENSP00000503874.1:p.Asp231Val
ENST00000678920.1:n.925A>T
ENST00000679019.1:n.1537A>T
ENST00000679117.1:c.*582A>T	ENSP00000503240.1:n.*582A>T
ENST00000679339.1:n.1608A>T
ENST00000326739.8:c.767A>T	ENSP00000321584.4:p.Asp256Val
ENST00000429182.5:c.561A>T
ENST00000442157.1:c.692A>T	ENSP00000403502.1:p.Asp231Val
ENST00000462980.1:n.669A>T
ENST00000491610.1:n.727A>T
NM_000884.2:c.767A>T	NP_000875.2:p.Asp256Val
XM_006713128.2:c.977A>T	XP_006713191.1:p.Asp326Val
XM_006713128.3:c.977A>T	XP_006713191.1:p.Asp326Val
XM_017006349.1:c.902A>T	XP_016861838.1:p.Asp301Val
XM_017006350.1:c.902A>T	XP_016861839.1:p.Asp301Val
NM_000884.3:c.767A>T MANE Select	NP_000875.2:p.Asp256Val