Canonical Allele Identifier: CA16602358

Gene: NRAS

Linked Data

• ClinVar Variation Id: 375871
• ClinVar RCV Id: RCV000426637 ; RCV000436751 ; RCV000443672
• dbSNP Id: rs121913255
• COSMIC: COSM586
• MyVariant Identifiers: chr1:g.115256528T>G (hg19) ; chr1:g.114713907T>G (hg38)
• CIViC: CA16602358
• PubMed: PMID:2674680 ; PMID:8120410 ; PMID:12460918 ; PMID:16291983 ; PMID:18390968 ; PMID:18948947 ; PMID:19657110 ; PMID:20130576 ; PMID:20179705 ; PMID:22761467 ; PMID:23076151 ; PMID:23414587 ; PMID:23515407 ; PMID:23538902 ; PMID:23569304 ; PMID:23614898 ; PMID:25157968

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713907T>G , CM000663.2:g.114713907T>G	GRCh38
NC_000001.10:g.115256528T>G , CM000663.1:g.115256528T>G	GRCh37
NC_000001.9:g.115058051T>G	NCBI36
NG_007572.1:g.7988A>C , LRG_92:g.7988A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.183A>C MANE Select	ENSP00000358548.4:p.Gln61His
ENST00000369535.4:c.183A>C	ENSP00000358548.4:p.Gln61His
NM_002524.4:c.183A>C	NP_002515.1:p.Gln61His
NM_002524.5:c.183A>C MANE Select	NP_002515.1:p.Gln61His