Canonical Allele Identifier: CA2575832584
Gene: IDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088550_90088551del , CM000677.2:g.90088550_90088551del GRCh38
NC_000015.9:g.90631782_90631783del , CM000677.1:g.90631782_90631783del GRCh37
NC_000015.8:g.88432786_88432787del NCBI36
NG_023302.1:g.18926_18927del , LRG_611:g.18926_18927del

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.534+36_534+37del MANE Select ENSP00000331897.4:n.534+36_534+37del
ENST00000330062.7:c.534+36_534+37del ENSP00000331897.3:n.534+36_534+37del
ENST00000540499.2:c.378+36_378+37del ENSP00000446147.2:n.378+36_378+37del
ENST00000559482.5:c.208-49_208-48del ENSP00000453016.1:n.208-49_208-48del
ENST00000560061.1:c.*159+36_*159+37del ENSP00000453254.1:n.*159+36_*159+37del
NM_001289910.1:c.378+36_378+37del , LRG_611t1:c.378+36_378+37del NP_001276839.1:n.378+36_378+37del
NM_001290114.1:c.144+36_144+37del NP_001277043.1:n.144+36_144+37del
NM_002168.3:c.534+36_534+37del , LRG_611t2:c.534+36_534+37del NP_002159.2:n.534+36_534+37del
NM_001290114.2:c.144+36_144+37del NP_001277043.1:n.144+36_144+37del
NM_002168.4:c.534+36_534+37del MANE Select NP_002159.2:n.534+36_534+37del