Canonical Allele Identifier: CA919615129

Gene: IDH2

Linked Data

• dbSNP Id: rs1596074597

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088606_90088607delinsAC , CM000677.2:g.90088606_90088607delinsAC	GRCh38
NC_000015.9:g.90631838_90631839delinsAC , CM000677.1:g.90631838_90631839delinsAC	GRCh37
NC_000015.8:g.88432842_88432843delinsAC	NCBI36
NG_023302.1:g.18870_18871delinsGT , LRG_611:g.18870_18871delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000330062.8:c.514_515delinsGT MANE Select	ENSP00000331897.4:p.Arg172Val
ENST00000330062.7:c.514_515delinsGT	ENSP00000331897.3:p.Arg172Val
ENST00000540499.2:c.358_359delinsGT	ENSP00000446147.2:p.Arg120Val
ENST00000559482.5:c.208-105_208-104delinsGT	ENSP00000453016.1:n.208-105_208-104delinsGT
ENST00000560061.1:c.*139_*140delinsGT	ENSP00000453254.1:n.*139_*140delinsGT
NM_001289910.1:c.358_359delinsGT , LRG_611t1:c.358_359delinsGT	NP_001276839.1:p.Arg120Val
NM_001290114.1:c.124_125delinsGT	NP_001277043.1:p.Arg42Val
NM_002168.3:c.514_515delinsGT , LRG_611t2:c.514_515delinsGT	NP_002159.2:p.Arg172Val
NM_001290114.2:c.124_125delinsGT	NP_001277043.1:p.Arg42Val
NM_002168.4:c.514_515delinsGT MANE Select	NP_002159.2:p.Arg172Val