Canonical Allele Identifier: CA393801929

Gene: IDH2

Linked Data

• gnomAD v4: 15-90088385-C-A
• MyVariant Identifiers: chr15:g.90631617C>A (hg19) ; chr15:g.90088385C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088385C>A , CM000677.2:g.90088385C>A	GRCh38
NC_000015.9:g.90631617C>A , CM000677.1:g.90631617C>A	GRCh37
NC_000015.8:g.88432621C>A	NCBI36
NG_023302.1:g.19092G>T , LRG_611:g.19092G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.652G>T MANE Select	ENSP00000331897.4:p.Gly218Cys
ENST00000330062.7:c.652G>T	ENSP00000331897.3:p.Gly218Cys
ENST00000540499.2:c.496G>T	ENSP00000446147.2:p.Gly166Cys
ENST00000559482.5:c.325G>T	ENSP00000453016.1:p.Gly109Cys
ENST00000560061.1:c.*277G>T	ENSP00000453254.1:n.*277G>T
NM_001289910.1:c.496G>T , LRG_611t1:c.496G>T	NP_001276839.1:p.Gly166Cys
NM_001290114.1:c.262G>T	NP_001277043.1:p.Gly88Cys
NM_002168.3:c.652G>T , LRG_611t2:c.652G>T	NP_002159.2:p.Gly218Cys
NM_001290114.2:c.262G>T	NP_001277043.1:p.Gly88Cys
NM_002168.4:c.652G>T MANE Select	NP_002159.2:p.Gly218Cys