Canonical Allele Identifier: CA7732921
Community Standard Title: NM_002168.4(IDH2):c.1206C>T (p.Cys402=)
Gene: IDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90084881G>A , CM000677.2:g.90084881G>A GRCh38
NC_000015.9:g.90628113G>A , CM000677.1:g.90628113G>A GRCh37
NC_000015.8:g.88429117G>A NCBI36
NG_023302.1:g.22596C>T , LRG_611:g.22596C>T

Transcript Alleles

HGVS Amino-acid Change
NM_002168.4:c.1206C>T MANE Select NP_002159.2:p.Cys402=
ENST00000330062.8:c.1206C>T MANE Select ENSP00000331897.4:p.Cys402=
NM_001289910.1:c.1050C>T , LRG_611t1:c.1050C>T NP_001276839.1:p.Cys350=
NM_001290114.1:c.816C>T NP_001277043.1:p.Cys272=
NM_001290114.2:c.816C>T NP_001277043.1:p.Cys272=
NM_002168.3:c.1206C>T , LRG_611t2:c.1206C>T NP_002159.2:p.Cys402=
ENST00000330062.7:c.1206C>T ENSP00000331897.3:p.Cys402=
ENST00000540499.2:c.1050C>T ENSP00000446147.2:p.Cys350=
ENST00000559482.5:c.851+120C>T ENSP00000453016.1:n.851+120C>T
ENST00000560061.1:c.*831C>T ENSP00000453254.1:n.*831C>T