Canonical Allele Identifier: CA2805186144

Gene: IDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088400_90088401insCCGATGAGCACCACCGACAGGGCGCCGGTCGCGGAGCCCACCGTGAAGCCGATAATATCCGGCGAACCCAGAGCATTGCGCGACACCGACTG , CM000677.2:g.90088400_90088401insCCGATGAGCACCACCGACAGGGCGCCGGTCGCGGAGCCCACCGTGAAGCCGATAATATCCGGCGAACCCAGAGCATTGCGCGACACCGACTG	GRCh38
NC_000015.9:g.90631632_90631633insCCGATGAGCACCACCGACAGGGCGCCGGTCGCGGAGCCCACCGTGAAGCCGATAATATCCGGCGAACCCAGAGCATTGCGCGACACCGACTG , CM000677.1:g.90631632_90631633insCCGATGAGCACCACCGACAGGGCGCCGGTCGCGGAGCCCACCGTGAAGCCGATAATATCCGGCGAACCCAGAGCATTGCGCGACACCGACTG	GRCh37
NC_000015.8:g.88432636_88432637insCCGATGAGCACCACCGACAGGGCGCCGGTCGCGGAGCCCACCGTGAAGCCGATAATATCCGGCGAACCCAGAGCATTGCGCGACACCGACTG	NCBI36
NG_023302.1:g.19077_19078insAGTCGGTGTCGCGCAATGCTCTGGGTTCGCCGGATATTATCGGCTTCACGGTGGGCTCCGCGACCGGCGCCCTGTCGGTGGTGCTCATCGGC , LRG_611:g.19077_19078insAGTCGGTGTCGCGCAATGCTCTGGGTTCGCCGGATATTATCGGCTTCACGGTGGGCTCCGCGACCGGCGCCCTGTCGGTGGTGCTCATCGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.637_638insAGTCGGTGTCGCGCAATGCTCTGGGTTCGCCGGATATTATCGGCTTCACGGTGGGCTCCGCGACCGGCGCCCTGTCGGTGGTGCTCATCGGC MANE Select	ENSP00000331897.4:p.Pro213GlnfsTer?
ENST00000330062.7:c.637_638insAGTCGGTGTCGCGCAATGCTCTGGGTTCGCCGGATATTATCGGCTTCACGGTGGGCTCCGCGACCGGCGCCCTGTCGGTGGTGCTCATCGGC	ENSP00000331897.3:p.Pro213GlnfsTer?
ENST00000540499.2:c.481_482insAGTCGGTGTCGCGCAATGCTCTGGGTTCGCCGGATATTATCGGCTTCACGGTGGGCTCCGCGACCGGCGCCCTGTCGGTGGTGCTCATCGGC	ENSP00000446147.2:p.Pro161GlnfsTer?
ENST00000559482.5:c.310_311insAGTCGGTGTCGCGCAATGCTCTGGGTTCGCCGGATATTATCGGCTTCACGGTGGGCTCCGCGACCGGCGCCCTGTCGGTGGTGCTCATCGGC	ENSP00000453016.1:p.Pro104GlnfsTer?
ENST00000560061.1:c.*262_*263insAGTCGGTGTCGCGCAATGCTCTGGGTTCGCCGGATATTATCGGCTTCACGGTGGGCTCCGCGACCGGCGCCCTGTCGGTGGTGCTCATCGGC	ENSP00000453254.1:n.*262_*263insAGTCGGTGTCGCGCAATGCTCTGGGTTCG...
NM_001289910.1:c.481_482insAGTCGGTGTCGCGCAATGCTCTGGGTTCGCCGGATATTATCGGCTTCACGGTGGGCTCCGCGACCGGCGCCCTGTCGGTGGTGCTCATCGGC , LRG_611t1:c.481_482insAGTCGGTGTCGCGCAATGCTCTGGGTTCGCCGGATATTATCGGCTTCACGGTGGGCTCCGCGACCGGCGCCCTGTCGGTGGTGCTCATCGGC	NP_001276839.1:p.Pro161GlnfsTer?
NM_001290114.1:c.247_248insAGTCGGTGTCGCGCAATGCTCTGGGTTCGCCGGATATTATCGGCTTCACGGTGGGCTCCGCGACCGGCGCCCTGTCGGTGGTGCTCATCGGC	NP_001277043.1:p.Pro83GlnfsTer?
NM_002168.3:c.637_638insAGTCGGTGTCGCGCAATGCTCTGGGTTCGCCGGATATTATCGGCTTCACGGTGGGCTCCGCGACCGGCGCCCTGTCGGTGGTGCTCATCGGC , LRG_611t2:c.637_638insAGTCGGTGTCGCGCAATGCTCTGGGTTCGCCGGATATTATCGGCTTCACGGTGGGCTCCGCGACCGGCGCCCTGTCGGTGGTGCTCATCGGC	NP_002159.2:p.Pro213GlnfsTer?
NM_001290114.2:c.247_248insAGTCGGTGTCGCGCAATGCTCTGGGTTCGCCGGATATTATCGGCTTCACGGTGGGCTCCGCGACCGGCGCCCTGTCGGTGGTGCTCATCGGC	NP_001277043.1:p.Pro83GlnfsTer?
NM_002168.4:c.637_638insAGTCGGTGTCGCGCAATGCTCTGGGTTCGCCGGATATTATCGGCTTCACGGTGGGCTCCGCGACCGGCGCCCTGTCGGTGGTGCTCATCGGC MANE Select	NP_002159.2:p.Pro213GlnfsTer?