Canonical Allele Identifier: CA280928

Gene: NRAS

Linked Data

• ClinVar Variation Id: 219097
• ClinVar RCV Id: RCV001813426
• dbSNP Id: rs121913237
• gnomAD v4: 1-114716126-C-G
• COSMIC: COSM565
• MyVariant Identifiers: chr1:g.115258747C>G (hg19) ; chr1:g.114716126C>G (hg38)
• PubMed: PMID:2674680 ; PMID:8120410 ; PMID:12460918 ; PMID:15951308 ; PMID:16273091 ; PMID:16291983 ; PMID:17699718 ; PMID:18390968 ; PMID:18948947 ; PMID:20130576 ; PMID:20179705 ; PMID:20619739 ; PMID:20736745 ; PMID:21305640 ; PMID:21729679 ; PMID:21829508 ; PMID:23414587 ; PMID:23515407 ; PMID:25157968 ; PMID:26619011

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114716126C>G , CM000663.2:g.114716126C>G	GRCh38
NC_000001.10:g.115258747C>G , CM000663.1:g.115258747C>G	GRCh37
NC_000001.9:g.115060270C>G	NCBI36
NG_007572.1:g.5769G>C , LRG_92:g.5769G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000369535.5:c.35G>C MANE Select	ENSP00000358548.4:p.Gly12Ala
ENST00000369535.4:c.35G>C	ENSP00000358548.4:p.Gly12Ala
NM_002524.4:c.35G>C	NP_002515.1:p.Gly12Ala
NM_002524.5:c.35G>C MANE Select	NP_002515.1:p.Gly12Ala