Canonical Allele Identifier: CA393802085
Gene: IDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088457T>G , CM000677.2:g.90088457T>G GRCh38
NC_000015.9:g.90631689T>G , CM000677.1:g.90631689T>G GRCh37
NC_000015.8:g.88432693T>G NCBI36
NG_023302.1:g.19020A>C , LRG_611:g.19020A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.580A>C MANE Select ENSP00000331897.4:p.Met194Leu
ENST00000330062.7:c.580A>C ENSP00000331897.3:p.Met194Leu
ENST00000540499.2:c.424A>C ENSP00000446147.2:p.Met142Leu
ENST00000559482.5:c.253A>C ENSP00000453016.1:p.Met85Leu
ENST00000560061.1:c.*205A>C ENSP00000453254.1:n.*205A>C
NM_001289910.1:c.424A>C , LRG_611t1:c.424A>C NP_001276839.1:p.Met142Leu
NM_001290114.1:c.190A>C NP_001277043.1:p.Met64Leu
NM_002168.3:c.580A>C , LRG_611t2:c.580A>C NP_002159.2:p.Met194Leu
NM_001290114.2:c.190A>C NP_001277043.1:p.Met64Leu
NM_002168.4:c.580A>C MANE Select NP_002159.2:p.Met194Leu