Canonical Allele Identifier: CA433629701

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064297T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026864T>C , CM000665.2:g.49026864T>C	GRCh38
NC_000003.11:g.49064297T>C , CM000665.1:g.49064297T>C	GRCh37
NC_000003.10:g.49039301T>C	NCBI36
NG_012091.1:g.7579A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2682A>G	ENSP00000515567.1:p.Glu894=
ENST00000703937.1:c.*1743A>G	ENSP00000515568.1:n.*1743A>G
ENST00000326739.9:c.642A>G MANE Select	ENSP00000321584.4:p.Glu214=
ENST00000429182.6:c.642A>G	ENSP00000393525.2:p.Glu214=
ENST00000442157.2:c.567A>G	ENSP00000403502.2:p.Glu189=
ENST00000462980.2:n.1157A>G
ENST00000472328.2:n.708A>G
ENST00000491610.2:n.602A>G
ENST00000676607.1:n.938A>G
ENST00000676627.1:n.1372A>G
ENST00000676708.1:n.1922A>G
ENST00000676864.1:n.1791A>G
ENST00000677010.1:c.678A>G	ENSP00000503089.1:p.Glu226=
ENST00000677108.1:n.2548A>G
ENST00000677168.1:n.1114A>G
ENST00000677185.1:n.1205A>G
ENST00000677205.1:n.1426A>G
ENST00000677344.1:n.1916A>G
ENST00000677480.1:c.*319A>G	ENSP00000504378.1:n.*319A>G
ENST00000677519.1:n.1352A>G
ENST00000677593.1:n.1198A>G
ENST00000677740.1:n.2147A>G
ENST00000677991.1:n.1815A>G
ENST00000678001.1:n.1135A>G
ENST00000678085.1:n.1198A>G
ENST00000678177.1:n.2491A>G
ENST00000678603.1:n.1720A>G
ENST00000678724.1:c.567A>G	ENSP00000503874.1:p.Glu189=
ENST00000678920.1:n.800A>G
ENST00000679019.1:n.1412A>G
ENST00000679117.1:c.*457A>G	ENSP00000503240.1:n.*457A>G
ENST00000679339.1:n.1483A>G
ENST00000326739.8:c.642A>G	ENSP00000321584.4:p.Glu214=
ENST00000429182.5:c.436A>G
ENST00000442157.1:c.567A>G	ENSP00000403502.1:p.Glu189=
ENST00000462980.1:n.544A>G
ENST00000491610.1:n.602A>G
NM_000884.2:c.642A>G	NP_000875.2:p.Glu214=
XM_006713128.2:c.852A>G	XP_006713191.1:p.Glu284=
XM_006713128.3:c.852A>G	XP_006713191.1:p.Glu284=
XM_017006349.1:c.777A>G	XP_016861838.1:p.Glu259=
XM_017006350.1:c.777A>G	XP_016861839.1:p.Glu259=
NM_000884.3:c.642A>G MANE Select	NP_000875.2:p.Glu214=