Canonical Allele Identifier: CA1363291585

Gene: IMPDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026619_49026623delinsGAAGT , CM000665.2:g.49026619_49026623delinsGAAGT	GRCh38
NC_000003.11:g.49064052_49064056delinsGAAGT , CM000665.1:g.49064052_49064056delinsGAAGT	GRCh37
NC_000003.10:g.49039056_49039060delinsGAAGT	NCBI36
NG_012091.1:g.7820_7824delinsACTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2860-14_2860-10delinsACTTC	ENSP00000515567.1:n.2860-14_2860-10delinsACTTC
ENST00000703937.1:c.*1921-14_*1921-10delinsACTTC	ENSP00000515568.1:n.*1921-14_*1921-10delinsACTTC
ENST00000326739.9:c.820-14_820-10delinsACTTC MANE Select	ENSP00000321584.4:n.820-14_820-10delinsACTTC
ENST00000429182.6:c.820-14_820-10delinsACTTC	ENSP00000393525.2:n.820-14_820-10delinsACTTC
ENST00000442157.2:c.745-14_745-10delinsACTTC	ENSP00000403502.2:n.745-14_745-10delinsACTTC
ENST00000462980.2:n.1335-14_1335-10delinsACTTC
ENST00000472328.2:n.886-14_886-10delinsACTTC
ENST00000491610.2:n.780-14_780-10delinsACTTC
ENST00000676607.1:n.1116-14_1116-10delinsACTTC
ENST00000676627.1:n.1550-14_1550-10delinsACTTC
ENST00000676708.1:n.2100-14_2100-10delinsACTTC
ENST00000676864.1:n.1969-14_1969-10delinsACTTC
ENST00000677010.1:c.856-26_856-22delinsACTTC	ENSP00000503089.1:n.856-26_856-22delinsACTTC
ENST00000677108.1:n.2789_2793delinsACTTC
ENST00000677168.1:n.1292-14_1292-10delinsACTTC
ENST00000677185.1:n.1383-14_1383-10delinsACTTC
ENST00000677205.1:n.1604-14_1604-10delinsACTTC
ENST00000677344.1:n.2094-14_2094-10delinsACTTC
ENST00000677480.1:c.*497-14_*497-10delinsACTTC	ENSP00000504378.1:n.*497-14_*497-10delinsACTTC
ENST00000677519.1:n.1530-14_1530-10delinsACTTC
ENST00000677593.1:n.1376-14_1376-10delinsACTTC
ENST00000677740.1:n.2325-14_2325-10delinsACTTC
ENST00000677991.1:n.1993-14_1993-10delinsACTTC
ENST00000678001.1:n.1313-14_1313-10delinsACTTC
ENST00000678085.1:n.1439_1443delinsACTTC
ENST00000678177.1:n.2732_2736delinsACTTC
ENST00000678603.1:n.1898-14_1898-10delinsACTTC
ENST00000678724.1:c.745-14_745-10delinsACTTC	ENSP00000503874.1:n.745-14_745-10delinsACTTC
ENST00000678920.1:n.978-14_978-10delinsACTTC
ENST00000679019.1:n.1653_1657delinsACTTC
ENST00000679117.1:c.*635-14_*635-10delinsACTTC	ENSP00000503240.1:n.*635-14_*635-10delinsACTTC
ENST00000679339.1:n.1661-14_1661-10delinsACTTC
ENST00000326739.8:c.820-14_820-10delinsACTTC	ENSP00000321584.4:n.820-14_820-10delinsACTTC
ENST00000429182.5:c.614-14_614-10delinsACTTC
ENST00000442157.1:c.745-14_745-10delinsACTTC	ENSP00000403502.1:n.745-14_745-10delinsACTTC
ENST00000462980.1:n.722-14_722-10delinsACTTC
ENST00000491610.1:n.780-14_780-10delinsACTTC
NM_000884.2:c.820-14_820-10delinsACTTC	NP_000875.2:n.820-14_820-10delinsACTTC
XM_006713128.2:c.1030-14_1030-10delinsACTTC	XP_006713191.1:n.1030-14_1030-10delinsACTTC
XM_006713128.3:c.1030-14_1030-10delinsACTTC	XP_006713191.1:n.1030-14_1030-10delinsACTTC
XM_017006349.1:c.955-14_955-10delinsACTTC	XP_016861838.1:n.955-14_955-10delinsACTTC
XM_017006350.1:c.955-14_955-10delinsACTTC	XP_016861839.1:n.955-14_955-10delinsACTTC
NM_000884.3:c.820-14_820-10delinsACTTC MANE Select	NP_000875.2:n.820-14_820-10delinsACTTC