Canonical Allele Identifier: CA716979522

Gene: IDH2

Linked Data

• dbSNP Id: rs1293885726
• gnomAD v4: 15-90088282-AGAAAG-A
• MyVariant Identifiers: chr15:g.90631515_90631519del (hg19) ; chr15:g.90088283_90088287del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088288_90088292del , CM000677.2:g.90088288_90088292del	GRCh38
NC_000015.9:g.90631520_90631524del , CM000677.1:g.90631520_90631524del	GRCh37
NC_000015.8:g.88432524_88432528del	NCBI36
NG_023302.1:g.19190_19194del , LRG_611:g.19190_19194del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.678+72_678+76del MANE Select	ENSP00000331897.4:n.678+72_678+76del
ENST00000330062.7:c.678+72_678+76del	ENSP00000331897.3:n.678+72_678+76del
ENST00000540499.2:c.522+72_522+76del	ENSP00000446147.2:n.522+72_522+76del
ENST00000559482.5:c.351+72_351+76del	ENSP00000453016.1:n.351+72_351+76del
ENST00000560061.1:c.*303+72_*303+76del	ENSP00000453254.1:n.*303+72_*303+76del
NM_001289910.1:c.522+72_522+76del , LRG_611t1:c.522+72_522+76del	NP_001276839.1:n.522+72_522+76del
NM_001290114.1:c.288+72_288+76del	NP_001277043.1:n.288+72_288+76del
NM_002168.3:c.678+72_678+76del , LRG_611t2:c.678+72_678+76del	NP_002159.2:n.678+72_678+76del
NM_001290114.2:c.288+72_288+76del	NP_001277043.1:n.288+72_288+76del
NM_002168.4:c.678+72_678+76del MANE Select	NP_002159.2:n.678+72_678+76del