Canonical Allele Identifier: CA645532887
Gene: IDH1 HGNC NCBI

Linked Data

dbSNP Id: rs2124862655

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208248388_208248389delinsGA , CM000664.2:g.208248388_208248389delinsGA GRCh38
NC_000002.11:g.209113112_209113113delinsGA , CM000664.1:g.209113112_209113113delinsGA GRCh37
NC_000002.10:g.208821357_208821358delinsGA NCBI36
NG_023319.2:g.22686_22687delinsTC , LRG_610:g.22686_22687delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000345146.7:c.394_395delinsTC MANE Select ENSP00000260985.2:p.Arg132Ser
ENST00000345146.6:c.394_395delinsTC ENSP00000260985.2:p.Arg132Ser
ENST00000415282.5:c.394_395delinsTC ENSP00000391075.1:p.Arg132Ser
ENST00000415913.5:c.394_395delinsTC ENSP00000390265.1:p.Arg132Ser
ENST00000446179.5:c.394_395delinsTC ENSP00000410513.1:p.Arg132Ser
ENST00000462386.5:n.607_608delinsTC
NM_001282386.1:c.394_395delinsTC , LRG_610t3:c.394_395delinsTC NP_001269315.1:p.Arg132Ser
NM_001282387.1:c.394_395delinsTC , LRG_610t2:c.394_395delinsTC NP_001269316.1:p.Arg132Ser
NM_005896.3:c.394_395delinsTC , LRG_610t1:c.394_395delinsTC NP_005887.2:p.Arg132Ser
NM_005896.4:c.394_395delinsTC MANE Select NP_005887.2:p.Arg132Ser