Canonical Allele Identifier: CA151263

Gene: NRAS

Linked Data

• ClinVar Variation Id: 73058
• ClinVar RCV Id: RCV000114746 ; RCV000144964 ; RCV000425440 ; RCV000426976 ; RCV000428264 ; RCV000428499 ; RCV000436588 ; RCV000418269 ; RCV000418907 ; RCV000431313 ; RCV000434388 ; RCV000435041 ; RCV000441559 ; RCV000436806 ; RCV000423656 ; RCV000443974 ; RCV000444882 ; RCV000423012 ; RCV000433274 ; RCV000441348 ; RCV000444538 ; RCV000626456 ; RCV000696329 ; RCV000662267 ; 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)
• CIViC: CA151263
• 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

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