Canonical Allele Identifier: CA393802029

Gene: IDH2

Linked Data

• gnomAD v4: 15-90088431-A-T
• MyVariant Identifiers: chr15:g.90631663A>T (hg19) ; chr15:g.90088431A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088431A>T , CM000677.2:g.90088431A>T	GRCh38
NC_000015.9:g.90631663A>T , CM000677.1:g.90631663A>T	GRCh37
NC_000015.8:g.88432667A>T	NCBI36
NG_023302.1:g.19046T>A , LRG_611:g.19046T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.606T>A MANE Select	ENSP00000331897.4:p.Ser202Arg
ENST00000330062.7:c.606T>A	ENSP00000331897.3:p.Ser202Arg
ENST00000540499.2:c.450T>A	ENSP00000446147.2:p.Ser150Arg
ENST00000559482.5:c.279T>A	ENSP00000453016.1:p.Ser93Arg
ENST00000560061.1:c.*231T>A	ENSP00000453254.1:n.*231T>A
NM_001289910.1:c.450T>A , LRG_611t1:c.450T>A	NP_001276839.1:p.Ser150Arg
NM_001290114.1:c.216T>A	NP_001277043.1:p.Ser72Arg
NM_002168.3:c.606T>A , LRG_611t2:c.606T>A	NP_002159.2:p.Ser202Arg
NM_001290114.2:c.216T>A	NP_001277043.1:p.Ser72Arg
NM_002168.4:c.606T>A MANE Select	NP_002159.2:p.Ser202Arg