Canonical Allele Identifier: CA350100980

Gene: IDH1

Linked Data

• dbSNP Id: rs1688060762
• MyVariant Identifiers: chr2:g.209113104A>T (hg19) ; chr2:g.208248380A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208248380A>T , CM000664.2:g.208248380A>T	GRCh38
NC_000002.11:g.209113104A>T , CM000664.1:g.209113104A>T	GRCh37
NC_000002.10:g.208821349A>T	NCBI36
NG_023319.2:g.22695T>A , LRG_610:g.22695T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345146.7:c.403T>A MANE Select	ENSP00000260985.2:p.Tyr135Asn
ENST00000345146.6:c.403T>A	ENSP00000260985.2:p.Tyr135Asn
ENST00000415282.5:c.403T>A	ENSP00000391075.1:p.Tyr135Asn
ENST00000415913.5:c.403T>A	ENSP00000390265.1:p.Tyr135Asn
ENST00000446179.5:c.403T>A	ENSP00000410513.1:p.Tyr135Asn
ENST00000462386.5:n.616T>A
NM_001282386.1:c.403T>A , LRG_610t3:c.403T>A	NP_001269315.1:p.Tyr135Asn
NM_001282387.1:c.403T>A , LRG_610t2:c.403T>A	NP_001269316.1:p.Tyr135Asn
NM_005896.3:c.403T>A , LRG_610t1:c.403T>A	NP_005887.2:p.Tyr135Asn
NM_005896.4:c.403T>A MANE Select	NP_005887.2:p.Tyr135Asn