Canonical Allele Identifier: CA763947004

Gene: IDH1

Linked Data

• dbSNP Id: rs1465727039
• gnomAD v3: 2-208248138-A-G
• gnomAD v4: 2-208248138-A-G
• MyVariant Identifiers: chr2:g.209112862A>G (hg19) ; chr2:g.208248138A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208248138A>G , CM000664.2:g.208248138A>G	GRCh38
NC_000002.11:g.209112862A>G , CM000664.1:g.209112862A>G	GRCh37
NC_000002.10:g.208821107A>G	NCBI36
NG_023319.2:g.22937T>C , LRG_610:g.22937T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345146.7:c.414+231T>C MANE Select	ENSP00000260985.2:n.414+231T>C
ENST00000345146.6:c.414+231T>C	ENSP00000260985.2:n.414+231T>C
ENST00000415282.5:c.414+231T>C	ENSP00000391075.1:n.414+231T>C
ENST00000415913.5:c.414+231T>C	ENSP00000390265.1:n.414+231T>C
ENST00000446179.5:c.414+231T>C	ENSP00000410513.1:n.414+231T>C
ENST00000462386.5:n.858T>C
NM_001282386.1:c.414+231T>C , LRG_610t3:c.414+231T>C	NP_001269315.1:n.414+231T>C
NM_001282387.1:c.414+231T>C , LRG_610t2:c.414+231T>C	NP_001269316.1:n.414+231T>C
NM_005896.3:c.414+231T>C , LRG_610t1:c.414+231T>C	NP_005887.2:n.414+231T>C
NM_005896.4:c.414+231T>C MANE Select	NP_005887.2:n.414+231T>C