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UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA16602358
Gene: NRAS
HGNC
NCBI
Linked Data
ClinVar Variation Id:
375871
ClinVar RCV Id:
RCV000426637
RCV000436751
RCV000443672
dbSNP Id:
rs121913255
COSMIC:
COSM586
MyVariant Identifiers:
chr1:g.115256528T>G (hg19)
chr1:g.114713907T>G (hg38)
CIViC:
CA16602358
PubMed:
PMID:2674680
PMID:8120410
PMID:12460918
PMID:16291983
PMID:18390968
PMID:18948947
PMID:19657110
PMID:20130576
PMID:20179705
PMID:22761467
PMID:23076151
PMID:23414587
PMID:23515407
PMID:23538902
PMID:23569304
PMID:23614898
PMID:25157968
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.114713907T>G , CM000663.2:g.114713907T>G
GRCh38
NC_000001.10:g.115256528T>G , CM000663.1:g.115256528T>G
GRCh37
NC_000001.9:g.115058051T>G
NCBI36
NG_007572.1:g.7988A>C , LRG_92:g.7988A>C
Transcript Alleles
HGVS
Amino-acid change
ENST00000369535.5:c.183A>C
MANE Select
ENSP00000358548.4:p.Gln61His
ENST00000369535.4:c.183A>C
ENSP00000358548.4:p.Gln61His
NM_002524.4:c.183A>C
NP_002515.1:p.Gln61His
NM_002524.5:c.183A>C
MANE Select
NP_002515.1:p.Gln61His
Search 100 bp 5'
Search 100 bp 3'