Canonical Allele Identifier: CA151261

Gene: NRAS

Linked Data

• ClinVar Variation Id: 13899
• ClinVar RCV Id: RCV000014913 ; RCV000114743 ; RCV000419545 ; RCV000419583 ; RCV000427817 ; RCV000424942 ; RCV000426328 ; RCV000428963 ; RCV000437450 ; RCV000438070 ; RCV000434327 ; RCV000444449 ; RCV001781267
• dbSNP Id: rs121434595
• gnomAD v4: 1-114716124-C-G
• COSMIC: COSM569
• MyVariant Identifiers: chr1:g.115258745C>G (hg19) ; chr1:g.114716124C>G (hg38)
• PubMed: PMID:2674680 ; PMID:3102434 ; PMID:8120410 ; PMID:16291983 ; PMID:18390968 ; PMID:18633438 ; PMID:20130576 ; PMID:20179705 ; PMID:22962325 ; PMID:23414587 ; PMID:25157968 ; PMID:26619011
• CIViC: CA151261

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114716124C>G , CM000663.2:g.114716124C>G	GRCh38
NC_000001.10:g.115258745C>G , CM000663.1:g.115258745C>G	GRCh37
NC_000001.9:g.115060268C>G	NCBI36
NG_007572.1:g.5771G>C , LRG_92:g.5771G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.37G>C MANE Select	ENSP00000358548.4:p.Gly13Arg
ENST00000369535.4:c.37G>C	ENSP00000358548.4:p.Gly13Arg
NM_002524.4:c.37G>C	NP_002515.1:p.Gly13Arg
NM_002524.5:c.37G>C MANE Select	NP_002515.1:p.Gly13Arg