Canonical Allele Identifier: CA645572396

Gene: IDH2

Linked Data

• dbSNP Id: rs2151549554
• COSMIC: COSM256046

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088605_90088606delinsAT , CM000677.2:g.90088605_90088606delinsAT	GRCh38
NC_000015.9:g.90631837_90631838delinsAT , CM000677.1:g.90631837_90631838delinsAT	GRCh37
NC_000015.8:g.88432841_88432842delinsAT	NCBI36
NG_023302.1:g.18871_18872delinsAT , LRG_611:g.18871_18872delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000330062.8:c.515_516delinsAT MANE Select	ENSP00000331897.4:p.Arg172Asn
ENST00000330062.7:c.515_516delinsAT	ENSP00000331897.3:p.Arg172Asn
ENST00000540499.2:c.359_360delinsAT	ENSP00000446147.2:p.Arg120Asn
ENST00000559482.5:c.208-104_208-103delinsAT	ENSP00000453016.1:n.208-104_208-103delinsAT
ENST00000560061.1:c.*140_*141delinsAT	ENSP00000453254.1:n.*140_*141delinsAT
NM_001289910.1:c.359_360delinsAT , LRG_611t1:c.359_360delinsAT	NP_001276839.1:p.Arg120Asn
NM_001290114.1:c.125_126delinsAT	NP_001277043.1:p.Arg42Asn
NM_002168.3:c.515_516delinsAT , LRG_611t2:c.515_516delinsAT	NP_002159.2:p.Arg172Asn
NM_001290114.2:c.125_126delinsAT	NP_001277043.1:p.Arg42Asn
NM_002168.4:c.515_516delinsAT MANE Select	NP_002159.2:p.Arg172Asn