Canonical Allele Identifier: CA2630319229
Gene: IDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088355_90088358dup , CM000677.2:g.90088355_90088358dup GRCh38
NC_000015.9:g.90631587_90631590dup , CM000677.1:g.90631587_90631590dup GRCh37
NC_000015.8:g.88432591_88432594dup NCBI36
NG_023302.1:g.19120_19123dup , LRG_611:g.19120_19123dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.678+2_678+5dup MANE Select ENSP00000331897.4:n.678+2_678+5dup
ENST00000330062.7:c.678+2_678+5dup ENSP00000331897.3:n.678+2_678+5dup
ENST00000540499.2:c.522+2_522+5dup ENSP00000446147.2:n.522+2_522+5dup
ENST00000559482.5:c.351+2_351+5dup ENSP00000453016.1:n.351+2_351+5dup
ENST00000560061.1:c.*303+2_*303+5dup ENSP00000453254.1:n.*303+2_*303+5dup
NM_001289910.1:c.522+2_522+5dup , LRG_611t1:c.522+2_522+5dup NP_001276839.1:n.522+2_522+5dup
NM_001290114.1:c.288+2_288+5dup NP_001277043.1:n.288+2_288+5dup
NM_002168.3:c.678+2_678+5dup , LRG_611t2:c.678+2_678+5dup NP_002159.2:n.678+2_678+5dup
NM_001290114.2:c.288+2_288+5dup NP_001277043.1:n.288+2_288+5dup
NM_002168.4:c.678+2_678+5dup MANE Select NP_002159.2:n.678+2_678+5dup