Canonical Allele Identifier: CA10602732
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 280409
ClinVar RCV Id: RCV000291285 RCV000419053 RCV000419201 RCV000420302 RCV000421291 RCV000421496 RCV000426654 RCV000427746 RCV000428903 RCV000430000 RCV000431592 RCV000432170 RCV000434604 RCV000437312 RCV000437545 RCV000438468 RCV000439526 RCV000439765 RCV000444278 RCV000444660 RCV003155143
dbSNP Id: rs11554290
MyVariant Identifiers: chr1:g.115256529T>G (hg19) chr1:g.114713908T>G (hg38)
PubMed: PMID:2674680 PMID:8120410 PMID:16291983 PMID:18390968 PMID:20130576 PMID:20179705 PMID:22761467 PMID:23414587 PMID:23538902 PMID:23569304 PMID:23614898 PMID:24370118 PMID:25157968 PMID:26619011
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713908T>G , CM000663.2:g.114713908T>G GRCh38
NC_000001.10:g.115256529T>G , CM000663.1:g.115256529T>G GRCh37
NC_000001.9:g.115058052T>G NCBI36
NG_007572.1:g.7987A>C , LRG_92:g.7987A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.182A>C MANE Select ENSP00000358548.4:p.Gln61Pro
ENST00000369535.4:c.182A>C ENSP00000358548.4:p.Gln61Pro
NM_002524.4:c.182A>C NP_002515.1:p.Gln61Pro
NM_002524.5:c.182A>C MANE Select NP_002515.1:p.Gln61Pro
Search 100 bp 5'
Search 100 bp 3'