Canonical Allele Identifier: CA297020
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 40468
ClinVar RCV Id: RCV000158979 RCV000422059 RCV000422738 RCV000425805 RCV000432311 RCV000433830 RCV000435186 RCV000440380 RCV000444830 RCV000445013 RCV002291497
dbSNP Id: rs121913250
COSMIC: COSM562
MyVariant Identifiers: chr1:g.115258748C>A (hg19) chr1:g.114716127C>A (hg38)
CIViC: CA297020
PubMed: PMID:2278970 PMID:2674680 PMID:3122217 PMID:8120410 PMID:12460918 PMID:16273091 PMID:16291983 PMID:16434492 PMID:17699718 PMID:18390968 PMID:18948947 PMID:19075190 PMID:19657110 PMID:20130576 PMID:20179705 PMID:20619739 PMID:20736745 PMID:21305640 PMID:21729679 PMID:21829508 PMID:22407852 PMID:23414587 PMID:23515407 PMID:23614898 PMID:25157968 PMID:26619011
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114716127C>A , CM000663.2:g.114716127C>A GRCh38
NC_000001.10:g.115258748C>A , CM000663.1:g.115258748C>A GRCh37
NC_000001.9:g.115060271C>A NCBI36
NG_007572.1:g.5768G>T , LRG_92:g.5768G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.34G>T MANE Select ENSP00000358548.4:p.Gly12Cys
ENST00000369535.4:c.34G>T ENSP00000358548.4:p.Gly12Cys
NM_002524.4:c.34G>T NP_002515.1:p.Gly12Cys
NM_002524.5:c.34G>T MANE Select NP_002515.1:p.Gly12Cys
Search 100 bp 5'
Search 100 bp 3'