Canonical Allele Identifier: CA2194954300

Gene: IDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088326_90088327delinsAG , CM000677.2:g.90088326_90088327delinsAG	GRCh38
NC_000015.9:g.90631558_90631559delinsAG , CM000677.1:g.90631558_90631559delinsAG	GRCh37
NC_000015.8:g.88432562_88432563delinsAG	NCBI36
NG_023302.1:g.19150_19151delinsCT , LRG_611:g.19150_19151delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.678+32_678+33delinsCT MANE Select	ENSP00000331897.4:n.678+32_678+33delinsCT
ENST00000330062.7:c.678+32_678+33delinsCT	ENSP00000331897.3:n.678+32_678+33delinsCT
ENST00000540499.2:c.522+32_522+33delinsCT	ENSP00000446147.2:n.522+32_522+33delinsCT
ENST00000559482.5:c.351+32_351+33delinsCT	ENSP00000453016.1:n.351+32_351+33delinsCT
ENST00000560061.1:c.*303+32_*303+33delinsCT	ENSP00000453254.1:n.*303+32_*303+33delinsCT
NM_001289910.1:c.522+32_522+33delinsCT , LRG_611t1:c.522+32_522+33delinsCT	NP_001276839.1:n.522+32_522+33delinsCT
NM_001290114.1:c.288+32_288+33delinsCT	NP_001277043.1:n.288+32_288+33delinsCT
NM_002168.3:c.678+32_678+33delinsCT , LRG_611t2:c.678+32_678+33delinsCT	NP_002159.2:n.678+32_678+33delinsCT
NM_001290114.2:c.288+32_288+33delinsCT	NP_001277043.1:n.288+32_288+33delinsCT
NM_002168.4:c.678+32_678+33delinsCT MANE Select	NP_002159.2:n.678+32_678+33delinsCT