Canonical Allele Identifier: CA1363291748

Gene: IMPDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026960_49026967delinsCCTTCTTG , CM000665.2:g.49026960_49026967delinsCCTTCTTG	GRCh38
NC_000003.11:g.49064393_49064400delinsCCTTCTTG , CM000665.1:g.49064393_49064400delinsCCTTCTTG	GRCh37
NC_000003.10:g.49039397_49039404delinsCCTTCTTG	NCBI36
NG_012091.1:g.7476_7483delinsCAAGAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2652_2659delinsCAAGAAGG	ENSP00000515567.1:p.Ser884=
ENST00000703937.1:c.*1713_*1720delinsCAAGAAGG	ENSP00000515568.1:n.*1713_*1720delinsCAAGAAGG
ENST00000326739.9:c.612_619delinsCAAGAAGG MANE Select	ENSP00000321584.4:p.Ser204=
ENST00000429182.6:c.612_619delinsCAAGAAGG	ENSP00000393525.2:p.Ser204=
ENST00000442157.2:c.537_544delinsCAAGAAGG	ENSP00000403502.2:p.Ser179=
ENST00000462980.2:n.1127_1134delinsCAAGAAGG
ENST00000472328.2:n.678_685delinsCAAGAAGG
ENST00000491610.2:n.499_506delinsCAAGAAGG
ENST00000676607.1:n.908_915delinsCAAGAAGG
ENST00000676627.1:n.1342_1349delinsCAAGAAGG
ENST00000676708.1:n.1819_1826delinsCAAGAAGG
ENST00000676864.1:n.1688_1695delinsCAAGAAGG
ENST00000677010.1:c.648_655delinsCAAGAAGG	ENSP00000503089.1:p.Ser216=
ENST00000677108.1:n.2445_2452delinsCAAGAAGG
ENST00000677168.1:n.1084_1091delinsCAAGAAGG
ENST00000677185.1:n.1102_1109delinsCAAGAAGG
ENST00000677205.1:n.1323_1330delinsCAAGAAGG
ENST00000677344.1:n.1813_1820delinsCAAGAAGG
ENST00000677480.1:c.*289_*296delinsCAAGAAGG	ENSP00000504378.1:n.*289_*296delinsCAAGAAGG
ENST00000677519.1:n.1322_1329delinsCAAGAAGG
ENST00000677593.1:n.1095_1102delinsCAAGAAGG
ENST00000677740.1:n.2044_2051delinsCAAGAAGG
ENST00000677991.1:n.1785_1792delinsCAAGAAGG
ENST00000678001.1:n.1105_1112delinsCAAGAAGG
ENST00000678085.1:n.1095_1102delinsCAAGAAGG
ENST00000678177.1:n.2388_2395delinsCAAGAAGG
ENST00000678603.1:n.1690_1697delinsCAAGAAGG
ENST00000678724.1:c.537_544delinsCAAGAAGG	ENSP00000503874.1:p.Ser179=
ENST00000678920.1:n.770_777delinsCAAGAAGG
ENST00000679019.1:n.1309_1316delinsCAAGAAGG
ENST00000679117.1:c.*427_*434delinsCAAGAAGG	ENSP00000503240.1:n.*427_*434delinsCAAGAAGG
ENST00000679339.1:n.1380_1387delinsCAAGAAGG
ENST00000326739.8:c.612_619delinsCAAGAAGG	ENSP00000321584.4:p.Ser204=
ENST00000429182.5:c.406_413delinsCAAGAAGG
ENST00000442157.1:c.537_544delinsCAAGAAGG	ENSP00000403502.1:p.Ser179=
ENST00000462980.1:n.514_521delinsCAAGAAGG
ENST00000491610.1:n.499_506delinsCAAGAAGG
NM_000884.2:c.612_619delinsCAAGAAGG	NP_000875.2:p.Ser204=
XM_006713128.2:c.822_829delinsCAAGAAGG	XP_006713191.1:p.Ser274=
XM_006713128.3:c.822_829delinsCAAGAAGG	XP_006713191.1:p.Ser274=
XM_017006349.1:c.747_754delinsCAAGAAGG	XP_016861838.1:p.Ser249=
XM_017006350.1:c.747_754delinsCAAGAAGG	XP_016861839.1:p.Ser249=
NM_000884.3:c.612_619delinsCAAGAAGG MANE Select	NP_000875.2:p.Ser204=