Canonical Allele Identifier: CA16602360
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 375873
ClinVar RCV Id: RCV000425830
dbSNP Id: rs1057519695
COSMIC: COSM33693
PubMed: PMID:2674680 PMID:8120410 PMID:16291983 PMID:18390968 PMID:20130576 PMID:20179705 PMID:22761467 PMID:23414587 PMID:23538902 PMID:23569304 PMID:23614898
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713907_114713908delinsCC , CM000663.2:g.114713907_114713908delinsCC GRCh38
NC_000001.10:g.115256528_115256529delinsCC , CM000663.1:g.115256528_115256529delinsCC GRCh37
NC_000001.9:g.115058051_115058052delinsCC NCBI36
NG_007572.1:g.7987_7988delinsGG , LRG_92:g.7987_7988delinsGG

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.182_183delinsGG MANE Select ENSP00000358548.4:p.Gln61Arg
ENST00000369535.4:c.182_183delinsGG ENSP00000358548.4:p.Gln61Arg
NM_002524.4:c.182_183delinsGG NP_002515.1:p.Gln61Arg
NM_002524.5:c.182_183delinsGG MANE Select NP_002515.1:p.Gln61Arg
Search 100 bp 5'
Search 100 bp 3'