Canonical Allele Identifier: CA16602363

Gene: NRAS

Linked Data

• ClinVar Variation Id: 375876
• ClinVar RCV Id: RCV000417850 ; RCV000423218 ; RCV000425977 ; RCV000432522 ; RCV000430805 ; RCV000435607 ; RCV000436237 ; RCV000437557 ; RCV000445025 ; RCV004022195 ; RCV000424444 ; RCV000444067
• dbSNP Id: rs121434596
• gnomAD v2: 1-115258744-C-A
• gnomAD v4: 1-114716123-C-A
• COSMIC: COSM574
• MyVariant Identifiers: chr1:g.115258744C>A (hg19) ; chr1:g.114716123C>A (hg38)
• PubMed: PMID:2674680 ; PMID:8120410 ; PMID:16291983 ; PMID:18390968 ; PMID:19657110 ; PMID:20130576 ; PMID:20179705 ; PMID:23414587 ; PMID:25157968 ; PMID:26619011

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114716123C>A , CM000663.2:g.114716123C>A	GRCh38
NC_000001.10:g.115258744C>A , CM000663.1:g.115258744C>A	GRCh37
NC_000001.9:g.115060267C>A	NCBI36
NG_007572.1:g.5772G>T , LRG_92:g.5772G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.38G>T MANE Select	ENSP00000358548.4:p.Gly13Val
ENST00000369535.4:c.38G>T	ENSP00000358548.4:p.Gly13Val
NM_002524.4:c.38G>T	NP_002515.1:p.Gly13Val
NM_002524.5:c.38G>T MANE Select	NP_002515.1:p.Gly13Val