Canonical Allele Identifier: CA297020

Gene: NRAS

Linked Data

• ClinVar Variation Id: 40468
• ClinVar RCV Id: RCV000158979 ; RCV000422059 ; RCV000422738 ; RCV000425805 ; RCV000433830 ; RCV000440380 ; RCV000435186 ; RCV000444830 ; RCV000432311 ; 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

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