Canonical Allele Identifier: CA2805186147

Gene: IDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088524_90088525insC , CM000677.2:g.90088524_90088525insC	GRCh38
NC_000015.9:g.90631756_90631757insC , CM000677.1:g.90631756_90631757insC	GRCh37
NC_000015.8:g.88432760_88432761insC	NCBI36
NG_023302.1:g.18952_18953insG , LRG_611:g.18952_18953insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.535-23_535-22insG MANE Select	ENSP00000331897.4:n.535-23_535-22insG
ENST00000330062.7:c.535-23_535-22insG	ENSP00000331897.3:n.535-23_535-22insG
ENST00000540499.2:c.379-23_379-22insG	ENSP00000446147.2:n.379-23_379-22insG
ENST00000559482.5:c.208-23_208-22insG	ENSP00000453016.1:n.208-23_208-22insG
ENST00000560061.1:c.*160-23_*160-22insG	ENSP00000453254.1:n.*160-23_*160-22insG
NM_001289910.1:c.379-23_379-22insG , LRG_611t1:c.379-23_379-22insG	NP_001276839.1:n.379-23_379-22insG
NM_001290114.1:c.145-23_145-22insG	NP_001277043.1:n.145-23_145-22insG
NM_002168.3:c.535-23_535-22insG , LRG_611t2:c.535-23_535-22insG	NP_002159.2:n.535-23_535-22insG
NM_001290114.2:c.145-23_145-22insG	NP_001277043.1:n.145-23_145-22insG
NM_002168.4:c.535-23_535-22insG MANE Select	NP_002159.2:n.535-23_535-22insG