Canonical Allele Identifier: CA123620

Gene: NRAS

Linked Data

• ClinVar Variation Id: 13901
• ClinVar RCV Id: RCV000014915 ; RCV000022690 ; RCV000144962 ; RCV000157672 ; RCV000431528 ; RCV000430350 ; RCV000433031 ; RCV000421906 ; RCV000440593 ; RCV000440357 ; RCV000421229 ; RCV000422699 ; RCV000431020 ; RCV000442419 ; RCV001293767
• dbSNP Id: rs121434596
• ExAC: 1:115258744 C / T
• gnomAD v2: 1-115258744-C-T
• gnomAD v4: 1-114716123-C-T
• COSMIC: COSM573
• MyVariant Identifiers: chr1:g.115258744C>T (hg19) ; chr1:g.114716123C>T (hg38)
• CIViC: CA123620
• PubMed: PMID:2407301 ; PMID:2674680 ; PMID:2989702 ; PMID:8120410 ; PMID:16291983 ; PMID:17332249 ; PMID:17517660 ; PMID:18375819 ; PMID:18390968 ; PMID:19657110 ; PMID:19775298 ; PMID:20130576 ; PMID:20179705 ; PMID:21079152 ; PMID:23414587 ; PMID:23431193 ; PMID:25157968 ; PMID:26619011

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.38G>A MANE Select	ENSP00000358548.4:p.Gly13Asp
ENST00000369535.4:c.38G>A	ENSP00000358548.4:p.Gly13Asp
NM_002524.4:c.38G>A	NP_002515.1:p.Gly13Asp
NM_002524.5:c.38G>A MANE Select	NP_002515.1:p.Gly13Asp