Canonical Allele Identifier: CA913184709
Gene: IDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088603_90088605delinsGCA , CM000677.2:g.90088603_90088605delinsGCA GRCh38
NC_000015.9:g.90631835_90631837delinsGCA , CM000677.1:g.90631835_90631837delinsGCA GRCh37
NC_000015.8:g.88432839_88432841delinsGCA NCBI36
NG_023302.1:g.18872_18874delinsTGC , LRG_611:g.18872_18874delinsTGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.516_518delinsTGC MANE Select ENSP00000331897.4:p.Arg172_His173delinsSerAla
ENST00000330062.7:c.516_518delinsTGC ENSP00000331897.3:p.Arg172_His173delinsSerAla
ENST00000540499.2:c.360_362delinsTGC ENSP00000446147.2:p.Arg120_His121delinsSerAla
ENST00000559482.5:c.208-103_208-101delinsTGC ENSP00000453016.1:n.208-103_208-101delinsTGC
ENST00000560061.1:c.*141_*143delinsTGC ENSP00000453254.1:n.*141_*143delinsTGC
NM_001289910.1:c.360_362delinsTGC , LRG_611t1:c.360_362delinsTGC NP_001276839.1:p.Arg120_His121delinsSerAla
NM_001290114.1:c.126_128delinsTGC NP_001277043.1:p.Arg42_His43delinsSerAla
NM_002168.3:c.516_518delinsTGC , LRG_611t2:c.516_518delinsTGC NP_002159.2:p.Arg172_His173delinsSerAla
NM_001290114.2:c.126_128delinsTGC NP_001277043.1:p.Arg42_His43delinsSerAla
NM_002168.4:c.516_518delinsTGC MANE Select NP_002159.2:p.Arg172_His173delinsSerAla