Canonical Allele Identifier: CA1363291700

Gene: IMPDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026875_49026876delinsTG , CM000665.2:g.49026875_49026876delinsTG	GRCh38
NC_000003.11:g.49064308_49064309delinsTG , CM000665.1:g.49064308_49064309delinsTG	GRCh37
NC_000003.10:g.49039312_49039313delinsTG	NCBI36
NG_012091.1:g.7567_7568delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2670_2671delinsCA	ENSP00000515567.1:p.Pro890=
ENST00000703937.1:c.*1731_*1732delinsCA	ENSP00000515568.1:n.*1731_*1732delinsCA
ENST00000326739.9:c.630_631delinsCA MANE Select	ENSP00000321584.4:p.Pro210=
ENST00000429182.6:c.630_631delinsCA	ENSP00000393525.2:p.Pro210=
ENST00000442157.2:c.555_556delinsCA	ENSP00000403502.2:p.Pro185=
ENST00000462980.2:n.1145_1146delinsCA
ENST00000472328.2:n.696_697delinsCA
ENST00000491610.2:n.590_591delinsCA
ENST00000676607.1:n.926_927delinsCA
ENST00000676627.1:n.1360_1361delinsCA
ENST00000676708.1:n.1910_1911delinsCA
ENST00000676864.1:n.1779_1780delinsCA
ENST00000677010.1:c.666_667delinsCA	ENSP00000503089.1:p.Pro222=
ENST00000677108.1:n.2536_2537delinsCA
ENST00000677168.1:n.1102_1103delinsCA
ENST00000677185.1:n.1193_1194delinsCA
ENST00000677205.1:n.1414_1415delinsCA
ENST00000677344.1:n.1904_1905delinsCA
ENST00000677480.1:c.*307_*308delinsCA	ENSP00000504378.1:n.*307_*308delinsCA
ENST00000677519.1:n.1340_1341delinsCA
ENST00000677593.1:n.1186_1187delinsCA
ENST00000677740.1:n.2135_2136delinsCA
ENST00000677991.1:n.1803_1804delinsCA
ENST00000678001.1:n.1123_1124delinsCA
ENST00000678085.1:n.1186_1187delinsCA
ENST00000678177.1:n.2479_2480delinsCA
ENST00000678603.1:n.1708_1709delinsCA
ENST00000678724.1:c.555_556delinsCA	ENSP00000503874.1:p.Pro185=
ENST00000678920.1:n.788_789delinsCA
ENST00000679019.1:n.1400_1401delinsCA
ENST00000679117.1:c.*445_*446delinsCA	ENSP00000503240.1:n.*445_*446delinsCA
ENST00000679339.1:n.1471_1472delinsCA
ENST00000326739.8:c.630_631delinsCA	ENSP00000321584.4:p.Pro210=
ENST00000429182.5:c.424_425delinsCA
ENST00000442157.1:c.555_556delinsCA	ENSP00000403502.1:p.Pro185=
ENST00000462980.1:n.532_533delinsCA
ENST00000491610.1:n.590_591delinsCA
NM_000884.2:c.630_631delinsCA	NP_000875.2:p.Pro210=
XM_006713128.2:c.840_841delinsCA	XP_006713191.1:p.Pro280=
XM_006713128.3:c.840_841delinsCA	XP_006713191.1:p.Pro280=
XM_017006349.1:c.765_766delinsCA	XP_016861838.1:p.Pro255=
XM_017006350.1:c.765_766delinsCA	XP_016861839.1:p.Pro255=
NM_000884.3:c.630_631delinsCA MANE Select	NP_000875.2:p.Pro210=