Canonical Allele Identifier: CA2194954391

Gene: IDH2

Linked Data

• dbSNP Id: rs1900935462
• gnomAD v4: 15-90088513-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088513_90088514insT , CM000677.2:g.90088513_90088514insT	GRCh38
NC_000015.9:g.90631745_90631746insT , CM000677.1:g.90631745_90631746insT	GRCh37
NC_000015.8:g.88432749_88432750insT	NCBI36
NG_023302.1:g.18963_18964insA , LRG_611:g.18963_18964insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.535-12_535-11insA MANE Select	ENSP00000331897.4:n.535-12_535-11insA
ENST00000330062.7:c.535-12_535-11insA	ENSP00000331897.3:n.535-12_535-11insA
ENST00000540499.2:c.379-12_379-11insA	ENSP00000446147.2:n.379-12_379-11insA
ENST00000559482.5:c.208-12_208-11insA	ENSP00000453016.1:n.208-12_208-11insA
ENST00000560061.1:c.*160-12_*160-11insA	ENSP00000453254.1:n.*160-12_*160-11insA
NM_001289910.1:c.379-12_379-11insA , LRG_611t1:c.379-12_379-11insA	NP_001276839.1:n.379-12_379-11insA
NM_001290114.1:c.145-12_145-11insA	NP_001277043.1:n.145-12_145-11insA
NM_002168.3:c.535-12_535-11insA , LRG_611t2:c.535-12_535-11insA	NP_002159.2:n.535-12_535-11insA
NM_001290114.2:c.145-12_145-11insA	NP_001277043.1:n.145-12_145-11insA
NM_002168.4:c.535-12_535-11insA MANE Select	NP_002159.2:n.535-12_535-11insA