Canonical Allele Identifier: CA2805186142
Gene: IDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088392_90088393insGTTGCGG , CM000677.2:g.90088392_90088393insGTTGCGG GRCh38
NC_000015.9:g.90631624_90631625insGTTGCGG , CM000677.1:g.90631624_90631625insGTTGCGG GRCh37
NC_000015.8:g.88432628_88432629insGTTGCGG NCBI36
NG_023302.1:g.19085_19086insCGCAACC , LRG_611:g.19085_19086insCGCAACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.645_646insCGCAACC MANE Select ENSP00000331897.4:p.Gly216ArgfsTer?
ENST00000330062.7:c.645_646insCGCAACC ENSP00000331897.3:p.Gly216ArgfsTer?
ENST00000540499.2:c.489_490insCGCAACC ENSP00000446147.2:p.Gly164ArgfsTer?
ENST00000559482.5:c.318_319insCGCAACC ENSP00000453016.1:p.Gly107ArgfsTer?
ENST00000560061.1:c.*270_*271insCGCAACC ENSP00000453254.1:n.*270_*271insCGCAACC
NM_001289910.1:c.489_490insCGCAACC , LRG_611t1:c.489_490insCGCAACC NP_001276839.1:p.Gly164ArgfsTer?
NM_001290114.1:c.255_256insCGCAACC NP_001277043.1:p.Gly86ArgfsTer?
NM_002168.3:c.645_646insCGCAACC , LRG_611t2:c.645_646insCGCAACC NP_002159.2:p.Gly216ArgfsTer?
NM_001290114.2:c.255_256insCGCAACC NP_001277043.1:p.Gly86ArgfsTer?
NM_002168.4:c.645_646insCGCAACC MANE Select NP_002159.2:p.Gly216ArgfsTer?