Canonical Allele Identifier: CA2841867228

Gene: IMPDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026623dup , CM000665.2:g.49026623dup	GRCh38
NC_000003.11:g.49064056dup , CM000665.1:g.49064056dup	GRCh37
NC_000003.10:g.49039060dup	NCBI36
NG_012091.1:g.7820dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2860-14dup	ENSP00000515567.1:n.2860-14dup
ENST00000703937.1:c.*1921-14dup	ENSP00000515568.1:n.*1921-14dup
ENST00000326739.9:c.820-14dup MANE Select	ENSP00000321584.4:n.820-14dup
ENST00000429182.6:c.820-14dup	ENSP00000393525.2:n.820-14dup
ENST00000442157.2:c.745-14dup	ENSP00000403502.2:n.745-14dup
ENST00000462980.2:n.1335-14dup
ENST00000472328.2:n.886-14dup
ENST00000491610.2:n.780-14dup
ENST00000676607.1:n.1116-14dup
ENST00000676627.1:n.1550-14dup
ENST00000676708.1:n.2100-14dup
ENST00000676864.1:n.1969-14dup
ENST00000677010.1:c.856-26dup	ENSP00000503089.1:n.856-26dup
ENST00000677108.1:n.2789dup
ENST00000677168.1:n.1292-14dup
ENST00000677185.1:n.1383-14dup
ENST00000677205.1:n.1604-14dup
ENST00000677344.1:n.2094-14dup
ENST00000677480.1:c.*497-14dup	ENSP00000504378.1:n.*497-14dup
ENST00000677519.1:n.1530-14dup
ENST00000677593.1:n.1376-14dup
ENST00000677740.1:n.2325-14dup
ENST00000677991.1:n.1993-14dup
ENST00000678001.1:n.1313-14dup
ENST00000678085.1:n.1439dup
ENST00000678177.1:n.2732dup
ENST00000678603.1:n.1898-14dup
ENST00000678724.1:c.745-14dup	ENSP00000503874.1:n.745-14dup
ENST00000678920.1:n.978-14dup
ENST00000679019.1:n.1653dup
ENST00000679117.1:c.*635-14dup	ENSP00000503240.1:n.*635-14dup
ENST00000679339.1:n.1661-14dup
ENST00000326739.8:c.820-14dup	ENSP00000321584.4:n.820-14dup
ENST00000429182.5:c.614-14dup
ENST00000442157.1:c.745-14dup	ENSP00000403502.1:n.745-14dup
ENST00000462980.1:n.722-14dup
ENST00000491610.1:n.780-14dup
NM_000884.2:c.820-14dup	NP_000875.2:n.820-14dup
XM_006713128.2:c.1030-14dup	XP_006713191.1:n.1030-14dup
XM_006713128.3:c.1030-14dup	XP_006713191.1:n.1030-14dup
XM_017006349.1:c.955-14dup	XP_016861838.1:n.955-14dup
XM_017006350.1:c.955-14dup	XP_016861839.1:n.955-14dup
NM_000884.3:c.820-14dup MANE Select	NP_000875.2:n.820-14dup