Canonical Allele Identifier: CA2194954301
Gene: IDH2 HGNC NCBI

Linked Data

dbSNP Id: rs1900927065

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088328del , CM000677.2:g.90088328del GRCh38
NC_000015.9:g.90631560del , CM000677.1:g.90631560del GRCh37
NC_000015.8:g.88432564del NCBI36
NG_023302.1:g.19150del , LRG_611:g.19150del

Transcript Alleles

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