Canonical Allele Identifier: CA352739607

Gene: IMPDH2

Linked Data

• COSMIC: COSM3373223
• MyVariant Identifiers: chr3:g.49064023G>C (hg19) ; chr3:g.49026590G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026590G>C , CM000665.2:g.49026590G>C	GRCh38
NC_000003.11:g.49064023G>C , CM000665.1:g.49064023G>C	GRCh37
NC_000003.10:g.49039027G>C	NCBI36
NG_012091.1:g.7853C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000703936.1:c.2879C>G	ENSP00000515567.1:p.Ser960Cys
ENST00000703937.1:c.*1940C>G	ENSP00000515568.1:n.*1940C>G
ENST00000326739.9:c.839C>G MANE Select	ENSP00000321584.4:p.Ser280Cys
ENST00000429182.6:c.839C>G	ENSP00000393525.2:p.Ser280Cys
ENST00000442157.2:c.764C>G	ENSP00000403502.2:p.Ser255Cys
ENST00000462980.2:n.1354C>G
ENST00000472328.2:n.905C>G
ENST00000491610.2:n.799C>G
ENST00000676607.1:n.1135C>G
ENST00000676627.1:n.1569C>G
ENST00000676708.1:n.2119C>G
ENST00000676864.1:n.1988C>G
ENST00000677010.1:c.863C>G	ENSP00000503089.1:p.Ser288Cys
ENST00000677108.1:n.2822C>G
ENST00000677168.1:n.1311C>G
ENST00000677185.1:n.1402C>G
ENST00000677205.1:n.1623C>G
ENST00000677344.1:n.2113C>G
ENST00000677480.1:c.*516C>G	ENSP00000504378.1:n.*516C>G
ENST00000677519.1:n.1549C>G
ENST00000677593.1:n.1395C>G
ENST00000677740.1:n.2344C>G
ENST00000677991.1:n.2012C>G
ENST00000678001.1:n.1332C>G
ENST00000678085.1:n.1472C>G
ENST00000678177.1:n.2765C>G
ENST00000678603.1:n.1917C>G
ENST00000678724.1:c.764C>G	ENSP00000503874.1:p.Ser255Cys
ENST00000678920.1:n.997C>G
ENST00000679019.1:n.1686C>G
ENST00000679117.1:c.*654C>G	ENSP00000503240.1:n.*654C>G
ENST00000679339.1:n.1680C>G
ENST00000326739.8:c.839C>G	ENSP00000321584.4:p.Ser280Cys
ENST00000429182.5:c.633C>G
ENST00000442157.1:c.764C>G	ENSP00000403502.1:p.Ser255Cys
ENST00000462980.1:n.741C>G
ENST00000491610.1:n.799C>G
NM_000884.2:c.839C>G	NP_000875.2:p.Ser280Cys
XM_006713128.2:c.1049C>G	XP_006713191.1:p.Ser350Cys
XM_006713128.3:c.1049C>G	XP_006713191.1:p.Ser350Cys
XM_017006349.1:c.974C>G	XP_016861838.1:p.Ser325Cys
XM_017006350.1:c.974C>G	XP_016861839.1:p.Ser325Cys
NM_000884.3:c.839C>G MANE Select	NP_000875.2:p.Ser280Cys