Canonical Allele Identifier: CA7732968
Community Standard Title: NM_002168.4(IDH2):c.1084C>T (p.Arg362Trp)
Gene: IDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90085095G>A , CM000677.2:g.90085095G>A GRCh38
NC_000015.9:g.90628327G>A , CM000677.1:g.90628327G>A GRCh37
NC_000015.8:g.88429331G>A NCBI36
NG_023302.1:g.22382C>T , LRG_611:g.22382C>T

Transcript Alleles

HGVS Amino-acid Change
NM_002168.4:c.1084C>T MANE Select NP_002159.2:p.Arg362Trp
ENST00000330062.8:c.1084C>T MANE Select ENSP00000331897.4:p.Arg362Trp
NM_001289910.1:c.928C>T , LRG_611t1:c.928C>T NP_001276839.1:p.Arg310Trp
NM_001290114.1:c.694C>T NP_001277043.1:p.Arg232Trp
NM_001290114.2:c.694C>T NP_001277043.1:p.Arg232Trp
NM_002168.3:c.1084C>T , LRG_611t2:c.1084C>T NP_002159.2:p.Arg362Trp
ENST00000330062.7:c.1084C>T ENSP00000331897.3:p.Arg362Trp
ENST00000540499.2:c.928C>T ENSP00000446147.2:p.Arg310Trp
ENST00000559482.5:c.757C>T ENSP00000453016.1:p.Arg253Trp
ENST00000560061.1:c.*709C>T ENSP00000453254.1:n.*709C>T