Canonical Allele Identifier: CA1363291689

Gene: IMPDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026855_49026858delinsCTCA , CM000665.2:g.49026855_49026858delinsCTCA	GRCh38
NC_000003.11:g.49064288_49064291delinsCTCA , CM000665.1:g.49064288_49064291delinsCTCA	GRCh37
NC_000003.10:g.49039292_49039295delinsCTCA	NCBI36
NG_012091.1:g.7585_7588delinsTGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2688_2691delinsTGAG	ENSP00000515567.1:p.Asp896=
ENST00000703937.1:c.*1749_*1752delinsTGAG	ENSP00000515568.1:n.*1749_*1752delinsTGAG
ENST00000326739.9:c.648_651delinsTGAG MANE Select	ENSP00000321584.4:p.Asp216=
ENST00000429182.6:c.648_651delinsTGAG	ENSP00000393525.2:p.Asp216=
ENST00000442157.2:c.573_576delinsTGAG	ENSP00000403502.2:p.Asp191=
ENST00000462980.2:n.1163_1166delinsTGAG
ENST00000472328.2:n.714_717delinsTGAG
ENST00000491610.2:n.608_611delinsTGAG
ENST00000676607.1:n.944_947delinsTGAG
ENST00000676627.1:n.1378_1381delinsTGAG
ENST00000676708.1:n.1928_1931delinsTGAG
ENST00000676864.1:n.1797_1800delinsTGAG
ENST00000677010.1:c.684_687delinsTGAG	ENSP00000503089.1:p.Asp228=
ENST00000677108.1:n.2554_2557delinsTGAG
ENST00000677168.1:n.1120_1123delinsTGAG
ENST00000677185.1:n.1211_1214delinsTGAG
ENST00000677205.1:n.1432_1435delinsTGAG
ENST00000677344.1:n.1922_1925delinsTGAG
ENST00000677480.1:c.*325_*328delinsTGAG	ENSP00000504378.1:n.*325_*328delinsTGAG
ENST00000677519.1:n.1358_1361delinsTGAG
ENST00000677593.1:n.1204_1207delinsTGAG
ENST00000677740.1:n.2153_2156delinsTGAG
ENST00000677991.1:n.1821_1824delinsTGAG
ENST00000678001.1:n.1141_1144delinsTGAG
ENST00000678085.1:n.1204_1207delinsTGAG
ENST00000678177.1:n.2497_2500delinsTGAG
ENST00000678603.1:n.1726_1729delinsTGAG
ENST00000678724.1:c.573_576delinsTGAG	ENSP00000503874.1:p.Asp191=
ENST00000678920.1:n.806_809delinsTGAG
ENST00000679019.1:n.1418_1421delinsTGAG
ENST00000679117.1:c.*463_*466delinsTGAG	ENSP00000503240.1:n.*463_*466delinsTGAG
ENST00000679339.1:n.1489_1492delinsTGAG
ENST00000326739.8:c.648_651delinsTGAG	ENSP00000321584.4:p.Asp216=
ENST00000429182.5:c.442_445delinsTGAG
ENST00000442157.1:c.573_576delinsTGAG	ENSP00000403502.1:p.Asp191=
ENST00000462980.1:n.550_553delinsTGAG
ENST00000491610.1:n.608_611delinsTGAG
NM_000884.2:c.648_651delinsTGAG	NP_000875.2:p.Asp216=
XM_006713128.2:c.858_861delinsTGAG	XP_006713191.1:p.Asp286=
XM_006713128.3:c.858_861delinsTGAG	XP_006713191.1:p.Asp286=
XM_017006349.1:c.783_786delinsTGAG	XP_016861838.1:p.Asp261=
XM_017006350.1:c.783_786delinsTGAG	XP_016861839.1:p.Asp261=
NM_000884.3:c.648_651delinsTGAG MANE Select	NP_000875.2:p.Asp216=