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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:
CA151261
Gene: NRAS
HGNC
NCBI
Linked Data
ClinVar Variation Id:
13899
ClinVar RCV Id:
RCV000014913
RCV000114743
RCV000419545
RCV000419583
RCV000424942
RCV000426328
RCV000427817
RCV000428963
RCV000434327
RCV000437450
RCV000438070
RCV000444449
RCV001781267
dbSNP Id:
rs121434595
gnomAD v4:
1-114716124-C-G
COSMIC:
COSM569
MyVariant Identifiers:
chr1:g.115258745C>G (hg19)
chr1:g.114716124C>G (hg38)
PubMed:
PMID:2674680
PMID:3102434
PMID:8120410
PMID:16291983
PMID:18390968
PMID:18633438
PMID:20130576
PMID:20179705
PMID:22962325
PMID:23414587
PMID:25157968
PMID:26619011
CIViC:
CA151261
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.114716124C>G , CM000663.2:g.114716124C>G
GRCh38
NC_000001.10:g.115258745C>G , CM000663.1:g.115258745C>G
GRCh37
NC_000001.9:g.115060268C>G
NCBI36
NG_007572.1:g.5771G>C , LRG_92:g.5771G>C
Transcript Alleles
HGVS
Amino-acid change
ENST00000369535.5:c.37G>C
MANE Select
ENSP00000358548.4:p.Gly13Arg
ENST00000369535.4:c.37G>C
ENSP00000358548.4:p.Gly13Arg
NM_002524.4:c.37G>C
NP_002515.1:p.Gly13Arg
NM_002524.5:c.37G>C
MANE Select
NP_002515.1:p.Gly13Arg
Search 100 bp 5'
Search 100 bp 3'