Canonical Allele Identifier: CA151263
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 73058
ClinVar RCV Id: RCV000114746 RCV000144964 RCV000418269 RCV000418907 RCV000423012 RCV000423656 RCV000425440 RCV000426976 RCV000428264 RCV000428499 RCV000431313 RCV000433274 RCV000434388 RCV000435041 RCV000436588 RCV000436806 RCV000441348 RCV000441559 RCV000443974 RCV000444538 RCV000444882 RCV000626456 RCV000662267 RCV000696329 RCV001092890
dbSNP Id: rs121913254
gnomAD v2: 1-115256530-G-T
gnomAD v4: 1-114713909-G-T
COSMIC: COSM580
MyVariant Identifiers: chr1:g.115256530G>T (hg19) chr1:g.114713909G>T (hg38)
PubMed: PMID:2674680 PMID:8120410 PMID:12460918 PMID:16273091 PMID:16291983 PMID:17699718 PMID:18390968 PMID:18633438 PMID:18948947 PMID:19657110 PMID:20130576 PMID:20179705 PMID:20619739 PMID:20736745 PMID:21107323 PMID:21305640 PMID:21729679 PMID:21829508 PMID:22761467 PMID:23392294 PMID:23414587 PMID:23515407 PMID:23538902 PMID:23569304 PMID:23614898 PMID:26619011 PMID:26821351
CIViC: CA151263
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713909G>T , CM000663.2:g.114713909G>T GRCh38
NC_000001.10:g.115256530G>T , CM000663.1:g.115256530G>T GRCh37
NC_000001.9:g.115058053G>T NCBI36
NG_007572.1:g.7986C>A , LRG_92:g.7986C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.181C>A MANE Select ENSP00000358548.4:p.Gln61Lys
ENST00000369535.4:c.181C>A ENSP00000358548.4:p.Gln61Lys
NM_002524.4:c.181C>A NP_002515.1:p.Gln61Lys
NM_002524.5:c.181C>A MANE Select NP_002515.1:p.Gln61Lys
Search 100 bp 5'
Search 100 bp 3'