Canonical Allele Identifier: CA2662867400
Gene: IDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208248255C>A , CM000664.2:g.208248255C>A GRCh38
NC_000002.11:g.209112979C>A , CM000664.1:g.209112979C>A GRCh37
NC_000002.10:g.208821224C>A NCBI36
NG_023319.2:g.22820G>T , LRG_610:g.22820G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000345146.7:c.414+114G>T MANE Select ENSP00000260985.2:n.414+114G>T
ENST00000345146.6:c.414+114G>T ENSP00000260985.2:n.414+114G>T
ENST00000415282.5:c.414+114G>T ENSP00000391075.1:n.414+114G>T
ENST00000415913.5:c.414+114G>T ENSP00000390265.1:n.414+114G>T
ENST00000446179.5:c.414+114G>T ENSP00000410513.1:n.414+114G>T
ENST00000462386.5:n.741G>T
NM_001282386.1:c.414+114G>T , LRG_610t3:c.414+114G>T NP_001269315.1:n.414+114G>T
NM_001282387.1:c.414+114G>T , LRG_610t2:c.414+114G>T NP_001269316.1:n.414+114G>T
NM_005896.3:c.414+114G>T , LRG_610t1:c.414+114G>T NP_005887.2:n.414+114G>T
NM_005896.4:c.414+114G>T MANE Select NP_005887.2:n.414+114G>T