Canonical Allele Identifier: CA2194954302

Gene: IDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088329_90088330delinsAG , CM000677.2:g.90088329_90088330delinsAG	GRCh38
NC_000015.9:g.90631561_90631562delinsAG , CM000677.1:g.90631561_90631562delinsAG	GRCh37
NC_000015.8:g.88432565_88432566delinsAG	NCBI36
NG_023302.1:g.19147_19148delinsCT , LRG_611:g.19147_19148delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.678+29_678+30delinsCT MANE Select	ENSP00000331897.4:n.678+29_678+30delinsCT
ENST00000330062.7:c.678+29_678+30delinsCT	ENSP00000331897.3:n.678+29_678+30delinsCT
ENST00000540499.2:c.522+29_522+30delinsCT	ENSP00000446147.2:n.522+29_522+30delinsCT
ENST00000559482.5:c.351+29_351+30delinsCT	ENSP00000453016.1:n.351+29_351+30delinsCT
ENST00000560061.1:c.*303+29_*303+30delinsCT	ENSP00000453254.1:n.*303+29_*303+30delinsCT
NM_001289910.1:c.522+29_522+30delinsCT , LRG_611t1:c.522+29_522+30delinsCT	NP_001276839.1:n.522+29_522+30delinsCT
NM_001290114.1:c.288+29_288+30delinsCT	NP_001277043.1:n.288+29_288+30delinsCT
NM_002168.3:c.678+29_678+30delinsCT , LRG_611t2:c.678+29_678+30delinsCT	NP_002159.2:n.678+29_678+30delinsCT
NM_001290114.2:c.288+29_288+30delinsCT	NP_001277043.1:n.288+29_288+30delinsCT
NM_002168.4:c.678+29_678+30delinsCT MANE Select	NP_002159.2:n.678+29_678+30delinsCT