Canonical Allele Identifier: CA257021

Gene: NRAS

Linked Data

• ClinVar Variation Id: 13903
• ClinVar RCV Id: RCV000014917 ; RCV000158982 ; RCV000208552 ; RCV001382056 ; RCV003415702
• dbSNP Id: rs267606920
• gnomAD v2: 1-115256532-C-T
• gnomAD v3: 1-114713911-C-T
• gnomAD v4: 1-114713911-C-T
• COSMIC: COSM28673
• MyVariant Identifiers: chr1:g.115256532C>T (hg19) ; chr1:g.114713911C>T (hg38)
• PubMed: PMID:19966803 ; PMID:20301303 ; PMID:26467218

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713911C>T , CM000663.2:g.114713911C>T	GRCh38
NC_000001.10:g.115256532C>T , CM000663.1:g.115256532C>T	GRCh37
NC_000001.9:g.115058055C>T	NCBI36
NG_007572.1:g.7984G>A , LRG_92:g.7984G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.179G>A MANE Select	ENSP00000358548.4:p.Gly60Glu
ENST00000369535.4:c.179G>A	ENSP00000358548.4:p.Gly60Glu
NM_002524.4:c.179G>A	NP_002515.1:p.Gly60Glu
NM_002524.5:c.179G>A MANE Select	NP_002515.1:p.Gly60Glu