Canonical Allele Identifier: CA123620
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 13901
ClinVar RCV Id: RCV000014915 RCV000022690 RCV000144962 RCV000157672 RCV000421229 RCV000421906 RCV000422699 RCV000430350 RCV000431020 RCV000431528 RCV000433031 RCV000440357 RCV000440593 RCV000442419 RCV001293767
dbSNP Id: rs121434596
ExAC: 1:115258744 C / T
gnomAD v2: 1-115258744-C-T
gnomAD v4: 1-114716123-C-T
COSMIC: COSM573
MyVariant Identifiers: chr1:g.115258744C>T (hg19) chr1:g.114716123C>T (hg38)
PubMed: PMID:2407301 PMID:2674680 PMID:2989702 PMID:8120410 PMID:16291983 PMID:17332249 PMID:17517660 PMID:18375819 PMID:18390968 PMID:19657110 PMID:19775298 PMID:20130576 PMID:20179705 PMID:21079152 PMID:23414587 PMID:23431193 PMID:25157968 PMID:26619011
CIViC: CA123620
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114716123C>T , CM000663.2:g.114716123C>T GRCh38
NC_000001.10:g.115258744C>T , CM000663.1:g.115258744C>T GRCh37
NC_000001.9:g.115060267C>T NCBI36
NG_007572.1:g.5772G>A , LRG_92:g.5772G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.38G>A MANE Select ENSP00000358548.4:p.Gly13Asp
ENST00000369535.4:c.38G>A ENSP00000358548.4:p.Gly13Asp
NM_002524.4:c.38G>A NP_002515.1:p.Gly13Asp
NM_002524.5:c.38G>A MANE Select NP_002515.1:p.Gly13Asp
Search 100 bp 5'
Search 100 bp 3'