Canonical Allele Identifier: CA16602359
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 375872
ClinVar RCV Id: RCV000443704
dbSNP Id: rs1057519695
COSMIC: COSM30646
PubMed: PMID:2674680 PMID:8120410 PMID:16291983 PMID:18390968 PMID:20130576 PMID:20149136 PMID:20179705 PMID:20406486 PMID:22761467 PMID:23414587 PMID:23538902 PMID:23569304 PMID:23614898 PMID:25157968
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713907_114713908delinsCA , CM000663.2:g.114713907_114713908delinsCA GRCh38
NC_000001.10:g.115256528_115256529delinsCA , CM000663.1:g.115256528_115256529delinsCA GRCh37
NC_000001.9:g.115058051_115058052delinsCA NCBI36
NG_007572.1:g.7987_7988delinsTG , LRG_92:g.7987_7988delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.182_183delinsTG MANE Select ENSP00000358548.4:p.Gln61Leu
ENST00000369535.4:c.182_183delinsTG ENSP00000358548.4:p.Gln61Leu
NM_002524.4:c.182_183delinsTG NP_002515.1:p.Gln61Leu
NM_002524.5:c.182_183delinsTG MANE Select NP_002515.1:p.Gln61Leu
Search 100 bp 5'
Search 100 bp 3'