Canonical Allele Identifier: CA1363291571

Gene: IMPDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026578_49026579delinsAT , CM000665.2:g.49026578_49026579delinsAT	GRCh38
NC_000003.11:g.49064011_49064012delinsAT , CM000665.1:g.49064011_49064012delinsAT	GRCh37
NC_000003.10:g.49039015_49039016delinsAT	NCBI36
NG_012091.1:g.7864_7865delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000703936.1:c.2890_2891delinsAT	ENSP00000515567.1:p.Ile964=
ENST00000703937.1:c.*1951_*1952delinsAT	ENSP00000515568.1:n.*1951_*1952delinsAT
ENST00000326739.9:c.850_851delinsAT MANE Select	ENSP00000321584.4:p.Ile284=
ENST00000429182.6:c.850_851delinsAT	ENSP00000393525.2:p.Ile284=
ENST00000442157.2:c.775_776delinsAT	ENSP00000403502.2:p.Ile259=
ENST00000462980.2:n.1365_1366delinsAT
ENST00000472328.2:n.916_917delinsAT
ENST00000491610.2:n.810_811delinsAT
ENST00000676607.1:n.1146_1147delinsAT
ENST00000676627.1:n.1580_1581delinsAT
ENST00000676708.1:n.2130_2131delinsAT
ENST00000676864.1:n.1999_2000delinsAT
ENST00000677010.1:c.874_875delinsAT	ENSP00000503089.1:p.Ile292=
ENST00000677108.1:n.2833_2834delinsAT
ENST00000677168.1:n.1322_1323delinsAT
ENST00000677185.1:n.1413_1414delinsAT
ENST00000677205.1:n.1634_1635delinsAT
ENST00000677344.1:n.2124_2125delinsAT
ENST00000677480.1:c.*527_*528delinsAT	ENSP00000504378.1:n.*527_*528delinsAT
ENST00000677519.1:n.1560_1561delinsAT
ENST00000677593.1:n.1406_1407delinsAT
ENST00000677740.1:n.2355_2356delinsAT
ENST00000677991.1:n.2023_2024delinsAT
ENST00000678001.1:n.1343_1344delinsAT
ENST00000678085.1:n.1483_1484delinsAT
ENST00000678177.1:n.2776_2777delinsAT
ENST00000678603.1:n.1928_1929delinsAT
ENST00000678724.1:c.775_776delinsAT	ENSP00000503874.1:p.Ile259=
ENST00000678920.1:n.1008_1009delinsAT
ENST00000679019.1:n.1697_1698delinsAT
ENST00000679117.1:c.*665_*666delinsAT	ENSP00000503240.1:n.*665_*666delinsAT
ENST00000679339.1:n.1691_1692delinsAT
ENST00000326739.8:c.850_851delinsAT	ENSP00000321584.4:p.Ile284=
ENST00000429182.5:c.644_645delinsAT
ENST00000442157.1:c.775_776delinsAT	ENSP00000403502.1:p.Ile259=
ENST00000462980.1:n.752_753delinsAT
ENST00000491610.1:n.810_811delinsAT
NM_000884.2:c.850_851delinsAT	NP_000875.2:p.Ile284=
XM_006713128.2:c.1060_1061delinsAT	XP_006713191.1:p.Ile354=
XM_006713128.3:c.1060_1061delinsAT	XP_006713191.1:p.Ile354=
XM_017006349.1:c.985_986delinsAT	XP_016861838.1:p.Ile329=
XM_017006350.1:c.985_986delinsAT	XP_016861839.1:p.Ile329=
NM_000884.3:c.850_851delinsAT MANE Select	NP_000875.2:p.Ile284=