Canonical Allele Identifier: CA2662867368

Gene: IDH1

Linked Data

• gnomAD v4: 2-208248235-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208248235T>C , CM000664.2:g.208248235T>C	GRCh38
NC_000002.11:g.209112959T>C , CM000664.1:g.209112959T>C	GRCh37
NC_000002.10:g.208821204T>C	NCBI36
NG_023319.2:g.22840A>G , LRG_610:g.22840A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345146.7:c.414+134A>G MANE Select	ENSP00000260985.2:n.414+134A>G
ENST00000345146.6:c.414+134A>G	ENSP00000260985.2:n.414+134A>G
ENST00000415282.5:c.414+134A>G	ENSP00000391075.1:n.414+134A>G
ENST00000415913.5:c.414+134A>G	ENSP00000390265.1:n.414+134A>G
ENST00000446179.5:c.414+134A>G	ENSP00000410513.1:n.414+134A>G
ENST00000462386.5:n.761A>G
NM_001282386.1:c.414+134A>G , LRG_610t3:c.414+134A>G	NP_001269315.1:n.414+134A>G
NM_001282387.1:c.414+134A>G , LRG_610t2:c.414+134A>G	NP_001269316.1:n.414+134A>G
NM_005896.3:c.414+134A>G , LRG_610t1:c.414+134A>G	NP_005887.2:n.414+134A>G
NM_005896.4:c.414+134A>G MANE Select	NP_005887.2:n.414+134A>G