Canonical Allele Identifier: CA2194954277

Gene: IDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088282_90088287delinsAGAAAG , CM000677.2:g.90088282_90088287delinsAGAAAG	GRCh38
NC_000015.9:g.90631514_90631519delinsAGAAAG , CM000677.1:g.90631514_90631519delinsAGAAAG	GRCh37
NC_000015.8:g.88432518_88432523delinsAGAAAG	NCBI36
NG_023302.1:g.19190_19195delinsCTTTCT , LRG_611:g.19190_19195delinsCTTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.678+72_678+77delinsCTTTCT MANE Select	ENSP00000331897.4:n.678+72_678+77delinsCTTTCT
ENST00000330062.7:c.678+72_678+77delinsCTTTCT	ENSP00000331897.3:n.678+72_678+77delinsCTTTCT
ENST00000540499.2:c.522+72_522+77delinsCTTTCT	ENSP00000446147.2:n.522+72_522+77delinsCTTTCT
ENST00000559482.5:c.351+72_351+77delinsCTTTCT	ENSP00000453016.1:n.351+72_351+77delinsCTTTCT
ENST00000560061.1:c.*303+72_*303+77delinsCTTTCT	ENSP00000453254.1:n.*303+72_*303+77delinsCTTTCT
NM_001289910.1:c.522+72_522+77delinsCTTTCT , LRG_611t1:c.522+72_522+77delinsCTTTCT	NP_001276839.1:n.522+72_522+77delinsCTTTCT
NM_001290114.1:c.288+72_288+77delinsCTTTCT	NP_001277043.1:n.288+72_288+77delinsCTTTCT
NM_002168.3:c.678+72_678+77delinsCTTTCT , LRG_611t2:c.678+72_678+77delinsCTTTCT	NP_002159.2:n.678+72_678+77delinsCTTTCT
NM_001290114.2:c.288+72_288+77delinsCTTTCT	NP_001277043.1:n.288+72_288+77delinsCTTTCT
NM_002168.4:c.678+72_678+77delinsCTTTCT MANE Select	NP_002159.2:n.678+72_678+77delinsCTTTCT