Canonical Allele Identifier: CA2194954288

Gene: IDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088301_90088303delinsCAG , CM000677.2:g.90088301_90088303delinsCAG	GRCh38
NC_000015.9:g.90631533_90631535delinsCAG , CM000677.1:g.90631533_90631535delinsCAG	GRCh37
NC_000015.8:g.88432537_88432539delinsCAG	NCBI36
NG_023302.1:g.19174_19176delinsCTG , LRG_611:g.19174_19176delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.678+56_678+58delinsCTG MANE Select	ENSP00000331897.4:n.678+56_678+58delinsCTG
ENST00000330062.7:c.678+56_678+58delinsCTG	ENSP00000331897.3:n.678+56_678+58delinsCTG
ENST00000540499.2:c.522+56_522+58delinsCTG	ENSP00000446147.2:n.522+56_522+58delinsCTG
ENST00000559482.5:c.351+56_351+58delinsCTG	ENSP00000453016.1:n.351+56_351+58delinsCTG
ENST00000560061.1:c.*303+56_*303+58delinsCTG	ENSP00000453254.1:n.*303+56_*303+58delinsCTG
NM_001289910.1:c.522+56_522+58delinsCTG , LRG_611t1:c.522+56_522+58delinsCTG	NP_001276839.1:n.522+56_522+58delinsCTG
NM_001290114.1:c.288+56_288+58delinsCTG	NP_001277043.1:n.288+56_288+58delinsCTG
NM_002168.3:c.678+56_678+58delinsCTG , LRG_611t2:c.678+56_678+58delinsCTG	NP_002159.2:n.678+56_678+58delinsCTG
NM_001290114.2:c.288+56_288+58delinsCTG	NP_001277043.1:n.288+56_288+58delinsCTG
NM_002168.4:c.678+56_678+58delinsCTG MANE Select	NP_002159.2:n.678+56_678+58delinsCTG