Canonical Allele Identifier: CA492298122
Community Standard Title: NM_002168.4(IDH2):c.432G>T (p.Gly144=)
Gene: IDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088689C>A , CM000677.2:g.90088689C>A GRCh38
NC_000015.9:g.90631921C>A , CM000677.1:g.90631921C>A GRCh37
NC_000015.8:g.88432925C>A NCBI36
NG_023302.1:g.18788G>T , LRG_611:g.18788G>T

Transcript Alleles

HGVS Amino-acid Change
NM_002168.4:c.432G>T MANE Select NP_002159.2:p.Gly144=
ENST00000330062.8:c.432G>T MANE Select ENSP00000331897.4:p.Gly144=
NM_001289910.1:c.276G>T , LRG_611t1:c.276G>T NP_001276839.1:p.Gly92=
NM_001290114.1:c.42G>T NP_001277043.1:p.Gly14=
NM_001290114.2:c.42G>T NP_001277043.1:p.Gly14=
NM_002168.3:c.432G>T , LRG_611t2:c.432G>T NP_002159.2:p.Gly144=
ENST00000330062.7:c.432G>T ENSP00000331897.3:p.Gly144=
ENST00000540499.2:c.276G>T ENSP00000446147.2:p.Gly92=
ENST00000559482.5:c.208-187G>T ENSP00000453016.1:n.208-187G>T
ENST00000560061.1:c.*57G>T ENSP00000453254.1:n.*57G>T