Canonical Allele Identifier: CA3250142882
Community Standard Title: NM_005896.4(IDH1):c.395_396delinsCA (p.Arg132Pro)
Gene: IDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208248387_208248388delinsTG , CM000664.2:g.208248387_208248388delinsTG GRCh38
NC_000002.11:g.209113111_209113112delinsTG , CM000664.1:g.209113111_209113112delinsTG GRCh37
NC_000002.10:g.208821356_208821357delinsTG NCBI36
NG_023319.2:g.22687_22688delinsCA , LRG_610:g.22687_22688delinsCA

Transcript Alleles

HGVS Amino-acid Change
NM_005896.4:c.395_396delinsCA MANE Select NP_005887.2:p.Arg132Pro
ENST00000345146.7:c.395_396delinsCA MANE Select ENSP00000260985.2:p.Arg132Pro
NM_001282386.1:c.395_396delinsCA , LRG_610t3:c.395_396delinsCA NP_001269315.1:p.Arg132Pro
NM_001282387.1:c.395_396delinsCA , LRG_610t2:c.395_396delinsCA NP_001269316.1:p.Arg132Pro
NM_005896.3:c.395_396delinsCA , LRG_610t1:c.395_396delinsCA NP_005887.2:p.Arg132Pro
ENST00000345146.6:c.395_396delinsCA ENSP00000260985.2:p.Arg132Pro
ENST00000415282.5:c.395_396delinsCA ENSP00000391075.1:p.Arg132Pro
ENST00000415913.5:c.395_396delinsCA ENSP00000390265.1:p.Arg132Pro
ENST00000446179.5:c.395_396delinsCA ENSP00000410513.1:p.Arg132Pro
ENST00000462386.5:n.608_609delinsCA