Canonical Allele Identifier: CA716979818

Gene: IDH2

Linked Data

• dbSNP Id: rs1410422146
• gnomAD v3: 15-90088492-GT-G
• gnomAD v4: 15-90088492-GT-G
• MyVariant Identifiers: chr15:g.90631725del (hg19) ; chr15:g.90088493del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088493del , CM000677.2:g.90088493del	GRCh38
NC_000015.9:g.90631725del , CM000677.1:g.90631725del	GRCh37
NC_000015.8:g.88432729del	NCBI36
NG_023302.1:g.18984del , LRG_611:g.18984del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.544del MANE Select	ENSP00000331897.4:p.Thr182GlnfsTer?
ENST00000330062.7:c.544del	ENSP00000331897.3:p.Thr182GlnfsTer?
ENST00000540499.2:c.388del	ENSP00000446147.2:p.Thr130GlnfsTer?
ENST00000559482.5:c.217del	ENSP00000453016.1:p.Thr73GlnfsTer?
ENST00000560061.1:c.*169del	ENSP00000453254.1:n.*169del
NM_001289910.1:c.388del , LRG_611t1:c.388del	NP_001276839.1:p.Thr130GlnfsTer?
NM_001290114.1:c.154del	NP_001277043.1:p.Thr52GlnfsTer?
NM_002168.3:c.544del , LRG_611t2:c.544del	NP_002159.2:p.Thr182GlnfsTer?
NM_001290114.2:c.154del	NP_001277043.1:p.Thr52GlnfsTer?
NM_002168.4:c.544del MANE Select	NP_002159.2:p.Thr182GlnfsTer?