Canonical Allele Identifier: CA352740559

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064238G>T (hg19) ; chr3:g.49026805G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026805G>T , CM000665.2:g.49026805G>T	GRCh38
NC_000003.11:g.49064238G>T , CM000665.1:g.49064238G>T	GRCh37
NC_000003.10:g.49039242G>T	NCBI36
NG_012091.1:g.7638C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2741C>A	ENSP00000515567.1:p.Pro914Gln
ENST00000703937.1:c.*1802C>A	ENSP00000515568.1:n.*1802C>A
ENST00000326739.9:c.701C>A MANE Select	ENSP00000321584.4:p.Pro234Gln
ENST00000429182.6:c.701C>A	ENSP00000393525.2:p.Pro234Gln
ENST00000442157.2:c.626C>A	ENSP00000403502.2:p.Pro209Gln
ENST00000462980.2:n.1216C>A
ENST00000472328.2:n.767C>A
ENST00000491610.2:n.661C>A
ENST00000676607.1:n.997C>A
ENST00000676627.1:n.1431C>A
ENST00000676708.1:n.1981C>A
ENST00000676864.1:n.1850C>A
ENST00000677010.1:c.737C>A	ENSP00000503089.1:p.Pro246Gln
ENST00000677108.1:n.2607C>A
ENST00000677168.1:n.1173C>A
ENST00000677185.1:n.1264C>A
ENST00000677205.1:n.1485C>A
ENST00000677344.1:n.1975C>A
ENST00000677480.1:c.*378C>A	ENSP00000504378.1:n.*378C>A
ENST00000677519.1:n.1411C>A
ENST00000677593.1:n.1257C>A
ENST00000677740.1:n.2206C>A
ENST00000677991.1:n.1874C>A
ENST00000678001.1:n.1194C>A
ENST00000678085.1:n.1257C>A
ENST00000678177.1:n.2550C>A
ENST00000678603.1:n.1779C>A
ENST00000678724.1:c.626C>A	ENSP00000503874.1:p.Pro209Gln
ENST00000678920.1:n.859C>A
ENST00000679019.1:n.1471C>A
ENST00000679117.1:c.*516C>A	ENSP00000503240.1:n.*516C>A
ENST00000679339.1:n.1542C>A
ENST00000326739.8:c.701C>A	ENSP00000321584.4:p.Pro234Gln
ENST00000429182.5:c.495C>A
ENST00000442157.1:c.626C>A	ENSP00000403502.1:p.Pro209Gln
ENST00000462980.1:n.603C>A
ENST00000491610.1:n.661C>A
NM_000884.2:c.701C>A	NP_000875.2:p.Pro234Gln
XM_006713128.2:c.911C>A	XP_006713191.1:p.Pro304Gln
XM_006713128.3:c.911C>A	XP_006713191.1:p.Pro304Gln
XM_017006349.1:c.836C>A	XP_016861838.1:p.Pro279Gln
XM_017006350.1:c.836C>A	XP_016861839.1:p.Pro279Gln
NM_000884.3:c.701C>A MANE Select	NP_000875.2:p.Pro234Gln