Canonical Allele Identifier: CA352741482

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064395T>C (hg19) ; chr3:g.49026962T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026962T>C , CM000665.2:g.49026962T>C	GRCh38
NC_000003.11:g.49064395T>C , CM000665.1:g.49064395T>C	GRCh37
NC_000003.10:g.49039399T>C	NCBI36
NG_012091.1:g.7481A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2657A>G	ENSP00000515567.1:p.Lys886Arg
ENST00000703937.1:c.*1718A>G	ENSP00000515568.1:n.*1718A>G
ENST00000326739.9:c.617A>G MANE Select	ENSP00000321584.4:p.Lys206Arg
ENST00000429182.6:c.617A>G	ENSP00000393525.2:p.Lys206Arg
ENST00000442157.2:c.542A>G	ENSP00000403502.2:p.Lys181Arg
ENST00000462980.2:n.1132A>G
ENST00000472328.2:n.683A>G
ENST00000491610.2:n.504A>G
ENST00000676607.1:n.913A>G
ENST00000676627.1:n.1347A>G
ENST00000676708.1:n.1824A>G
ENST00000676864.1:n.1693A>G
ENST00000677010.1:c.653A>G	ENSP00000503089.1:p.Lys218Arg
ENST00000677108.1:n.2450A>G
ENST00000677168.1:n.1089A>G
ENST00000677185.1:n.1107A>G
ENST00000677205.1:n.1328A>G
ENST00000677344.1:n.1818A>G
ENST00000677480.1:c.*294A>G	ENSP00000504378.1:n.*294A>G
ENST00000677519.1:n.1327A>G
ENST00000677593.1:n.1100A>G
ENST00000677740.1:n.2049A>G
ENST00000677991.1:n.1790A>G
ENST00000678001.1:n.1110A>G
ENST00000678085.1:n.1100A>G
ENST00000678177.1:n.2393A>G
ENST00000678603.1:n.1695A>G
ENST00000678724.1:c.542A>G	ENSP00000503874.1:p.Lys181Arg
ENST00000678920.1:n.775A>G
ENST00000679019.1:n.1314A>G
ENST00000679117.1:c.*432A>G	ENSP00000503240.1:n.*432A>G
ENST00000679339.1:n.1385A>G
ENST00000326739.8:c.617A>G	ENSP00000321584.4:p.Lys206Arg
ENST00000429182.5:c.411A>G
ENST00000442157.1:c.542A>G	ENSP00000403502.1:p.Lys181Arg
ENST00000462980.1:n.519A>G
ENST00000491610.1:n.504A>G
NM_000884.2:c.617A>G	NP_000875.2:p.Lys206Arg
XM_006713128.2:c.827A>G	XP_006713191.1:p.Lys276Arg
XM_006713128.3:c.827A>G	XP_006713191.1:p.Lys276Arg
XM_017006349.1:c.752A>G	XP_016861838.1:p.Lys251Arg
XM_017006350.1:c.752A>G	XP_016861839.1:p.Lys251Arg
NM_000884.3:c.617A>G MANE Select	NP_000875.2:p.Lys206Arg