Canonical Allele Identifier: CA2194954278
Gene: IDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088284_90088288delinsAAAGG , CM000677.2:g.90088284_90088288delinsAAAGG GRCh38
NC_000015.9:g.90631516_90631520delinsAAAGG , CM000677.1:g.90631516_90631520delinsAAAGG GRCh37
NC_000015.8:g.88432520_88432524delinsAAAGG NCBI36
NG_023302.1:g.19189_19193delinsCCTTT , LRG_611:g.19189_19193delinsCCTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.678+71_678+75delinsCCTTT MANE Select ENSP00000331897.4:n.678+71_678+75delinsCCTTT
ENST00000330062.7:c.678+71_678+75delinsCCTTT ENSP00000331897.3:n.678+71_678+75delinsCCTTT
ENST00000540499.2:c.522+71_522+75delinsCCTTT ENSP00000446147.2:n.522+71_522+75delinsCCTTT
ENST00000559482.5:c.351+71_351+75delinsCCTTT ENSP00000453016.1:n.351+71_351+75delinsCCTTT
ENST00000560061.1:c.*303+71_*303+75delinsCCTTT ENSP00000453254.1:n.*303+71_*303+75delinsCCTTT
NM_001289910.1:c.522+71_522+75delinsCCTTT , LRG_611t1:c.522+71_522+75delinsCCTTT NP_001276839.1:n.522+71_522+75delinsCCTTT
NM_001290114.1:c.288+71_288+75delinsCCTTT NP_001277043.1:n.288+71_288+75delinsCCTTT
NM_002168.3:c.678+71_678+75delinsCCTTT , LRG_611t2:c.678+71_678+75delinsCCTTT NP_002159.2:n.678+71_678+75delinsCCTTT
NM_001290114.2:c.288+71_288+75delinsCCTTT NP_001277043.1:n.288+71_288+75delinsCCTTT
NM_002168.4:c.678+71_678+75delinsCCTTT MANE Select NP_002159.2:n.678+71_678+75delinsCCTTT