Canonical Allele Identifier: CA2662867157

Gene: IDH1

Linked Data

• gnomAD v4: 2-208247933-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208247933A>G , CM000664.2:g.208247933A>G	GRCh38
NC_000002.11:g.209112657A>G , CM000664.1:g.209112657A>G	GRCh37
NC_000002.10:g.208820902A>G	NCBI36
NG_023319.2:g.23142T>C , LRG_610:g.23142T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345146.7:c.414+436T>C MANE Select	ENSP00000260985.2:n.414+436T>C
ENST00000345146.6:c.414+436T>C	ENSP00000260985.2:n.414+436T>C
ENST00000415282.5:c.414+436T>C	ENSP00000391075.1:n.414+436T>C
ENST00000415913.5:c.414+436T>C	ENSP00000390265.1:n.414+436T>C
ENST00000446179.5:c.414+436T>C	ENSP00000410513.1:n.414+436T>C
ENST00000462386.5:n.1063T>C
NM_001282386.1:c.414+436T>C , LRG_610t3:c.414+436T>C	NP_001269315.1:n.414+436T>C
NM_001282387.1:c.414+436T>C , LRG_610t2:c.414+436T>C	NP_001269316.1:n.414+436T>C
NM_005896.3:c.414+436T>C , LRG_610t1:c.414+436T>C	NP_005887.2:n.414+436T>C
NM_005896.4:c.414+436T>C MANE Select	NP_005887.2:n.414+436T>C