Canonical Allele Identifier: CA393802164

Gene: IDH2

Linked Data

• MyVariant Identifiers: chr15:g.90631727G>T (hg19) ; chr15:g.90088495G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088495G>T , CM000677.2:g.90088495G>T	GRCh38
NC_000015.9:g.90631727G>T , CM000677.1:g.90631727G>T	GRCh37
NC_000015.8:g.88432731G>T	NCBI36
NG_023302.1:g.18982C>A , LRG_611:g.18982C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.542C>A MANE Select	ENSP00000331897.4:p.Ala181Asp
ENST00000330062.7:c.542C>A	ENSP00000331897.3:p.Ala181Asp
ENST00000540499.2:c.386C>A	ENSP00000446147.2:p.Ala129Asp
ENST00000559482.5:c.215C>A	ENSP00000453016.1:p.Ala72Asp
ENST00000560061.1:c.*167C>A	ENSP00000453254.1:n.*167C>A
NM_001289910.1:c.386C>A , LRG_611t1:c.386C>A	NP_001276839.1:p.Ala129Asp
NM_001290114.1:c.152C>A	NP_001277043.1:p.Ala51Asp
NM_002168.3:c.542C>A , LRG_611t2:c.542C>A	NP_002159.2:p.Ala181Asp
NM_001290114.2:c.152C>A	NP_001277043.1:p.Ala51Asp
NM_002168.4:c.542C>A MANE Select	NP_002159.2:p.Ala181Asp