Canonical Allele Identifier: CA1323987992
Gene: IDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208247988_208247989delinsAC , CM000664.2:g.208247988_208247989delinsAC GRCh38
NC_000002.11:g.209112712_209112713delinsAC , CM000664.1:g.209112712_209112713delinsAC GRCh37
NC_000002.10:g.208820957_208820958delinsAC NCBI36
NG_023319.2:g.23086_23087delinsGT , LRG_610:g.23086_23087delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000345146.7:c.414+380_414+381delinsGT MANE Select ENSP00000260985.2:n.414+380_414+381delinsGT
ENST00000345146.6:c.414+380_414+381delinsGT ENSP00000260985.2:n.414+380_414+381delinsGT
ENST00000415282.5:c.414+380_414+381delinsGT ENSP00000391075.1:n.414+380_414+381delinsGT
ENST00000415913.5:c.414+380_414+381delinsGT ENSP00000390265.1:n.414+380_414+381delinsGT
ENST00000446179.5:c.414+380_414+381delinsGT ENSP00000410513.1:n.414+380_414+381delinsGT
ENST00000462386.5:n.1007_1008delinsGT
NM_001282386.1:c.414+380_414+381delinsGT , LRG_610t3:c.414+380_414+381delinsGT NP_001269315.1:n.414+380_414+381delinsGT
NM_001282387.1:c.414+380_414+381delinsGT , LRG_610t2:c.414+380_414+381delinsGT NP_001269316.1:n.414+380_414+381delinsGT
NM_005896.3:c.414+380_414+381delinsGT , LRG_610t1:c.414+380_414+381delinsGT NP_005887.2:n.414+380_414+381delinsGT
NM_005896.4:c.414+380_414+381delinsGT MANE Select NP_005887.2:n.414+380_414+381delinsGT