Canonical Allele Identifier: CA492297502

Gene: IDH2

Linked Data

• MyVariant Identifiers: chr15:g.90631675T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088443T>A , CM000677.2:g.90088443T>A	GRCh38
NC_000015.9:g.90631675T>A , CM000677.1:g.90631675T>A	GRCh37
NC_000015.8:g.88432679T>A	NCBI36
NG_023302.1:g.19034A>T , LRG_611:g.19034A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.594A>T MANE Select	ENSP00000331897.4:p.Pro198=
ENST00000330062.7:c.594A>T	ENSP00000331897.3:p.Pro198=
ENST00000540499.2:c.438A>T	ENSP00000446147.2:p.Pro146=
ENST00000559482.5:c.267A>T	ENSP00000453016.1:p.Pro89=
ENST00000560061.1:c.*219A>T	ENSP00000453254.1:n.*219A>T
NM_001289910.1:c.438A>T , LRG_611t1:c.438A>T	NP_001276839.1:p.Pro146=
NM_001290114.1:c.204A>T	NP_001277043.1:p.Pro68=
NM_002168.3:c.594A>T , LRG_611t2:c.594A>T	NP_002159.2:p.Pro198=
NM_001290114.2:c.204A>T	NP_001277043.1:p.Pro68=
NM_002168.4:c.594A>T MANE Select	NP_002159.2:p.Pro198=