Canonical Allele Identifier: CA645572395
Gene: IDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088605_90088606delinsTT , CM000677.2:g.90088605_90088606delinsTT GRCh38
NC_000015.9:g.90631837_90631838delinsTT , CM000677.1:g.90631837_90631838delinsTT GRCh37
NC_000015.8:g.88432841_88432842delinsTT NCBI36
NG_023302.1:g.18871_18872delinsAA , LRG_611:g.18871_18872delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.515_516delinsAA MANE Select ENSP00000331897.4:p.Arg172Lys
ENST00000330062.7:c.515_516delinsAA ENSP00000331897.3:p.Arg172Lys
ENST00000540499.2:c.359_360delinsAA ENSP00000446147.2:p.Arg120Lys
ENST00000559482.5:c.208-104_208-103delinsAA ENSP00000453016.1:n.208-104_208-103delinsAA
ENST00000560061.1:c.*140_*141delinsAA ENSP00000453254.1:n.*140_*141delinsAA
NM_001289910.1:c.359_360delinsAA , LRG_611t1:c.359_360delinsAA NP_001276839.1:p.Arg120Lys
NM_001290114.1:c.125_126delinsAA NP_001277043.1:p.Arg42Lys
NM_002168.3:c.515_516delinsAA , LRG_611t2:c.515_516delinsAA NP_002159.2:p.Arg172Lys
NM_001290114.2:c.125_126delinsAA NP_001277043.1:p.Arg42Lys
NM_002168.4:c.515_516delinsAA MANE Select NP_002159.2:p.Arg172Lys