Canonical Allele Identifier: CA180753
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 177778
ClinVar RCV Id: RCV000158978 RCV000212761 RCV000421327 RCV000421993 RCV000427184 RCV000430288 RCV000431995 RCV000433097 RCV000439216 RCV000442594 RCV000445150 RCV001066799
dbSNP Id: rs121913250
gnomAD v4: 1-114716127-C-T
COSMIC: COSM563
MyVariant Identifiers: chr1:g.115258748C>T (hg19) chr1:g.114716127C>T (hg38)
PubMed: PMID:2674680 PMID:8120410 PMID:10598665 PMID:12460918 PMID:16273091 PMID:16291983 PMID:16518851 PMID:17384584 PMID:17699718 PMID:18390968 PMID:18794081 PMID:19047918 PMID:19657110 PMID:19966803 PMID:20130576 PMID:20179705 PMID:20619739 PMID:20736745 PMID:21305640 PMID:21729679 PMID:21829508 PMID:23414587 PMID:25157968 PMID:26619011 PMID:28098151
CIViC: CA180753
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114716127C>T , CM000663.2:g.114716127C>T GRCh38
NC_000001.10:g.115258748C>T , CM000663.1:g.115258748C>T GRCh37
NC_000001.9:g.115060271C>T NCBI36
NG_007572.1:g.5768G>A , LRG_92:g.5768G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.34G>A MANE Select ENSP00000358548.4:p.Gly12Ser
ENST00000369535.4:c.34G>A ENSP00000358548.4:p.Gly12Ser
NM_002524.4:c.34G>A NP_002515.1:p.Gly12Ser
NM_002524.5:c.34G>A MANE Select NP_002515.1:p.Gly12Ser
Search 100 bp 5'
Search 100 bp 3'