Canonical Allele Identifier: CA16042285

Gene: NRAS

Linked Data

• ClinVar Variation Id: 373003
• ClinVar RCV Id: RCV000414646 ; RCV000418758 ; RCV000419887 ; RCV000420139 ; RCV000420910 ; RCV000422093 ; RCV000424220 ; RCV000427364 ; RCV000428418 ; RCV000429512 ; RCV000429704 ; RCV000431603 ; RCV000434043 ; RCV000436881 ; RCV000437158 ; RCV000438233 ; RCV000439006 ; RCV000439308 ; RCV000444600 ; RCV001813470
• dbSNP Id: rs121913255
• COSMIC: COSM585
• MyVariant Identifiers: chr1:g.115256528T>A (hg19) ; chr1:g.114713907T>A (hg38)
• PubMed: PMID:2674680 ; PMID:8120410 ; PMID:16291983 ; PMID:18390968 ; PMID:19657110 ; PMID:20130576 ; PMID:20179705 ; PMID:22761467 ; PMID:23076151 ; PMID:23414587 ; PMID:23538902 ; PMID:23569304 ; PMID:23614898 ; PMID:25157968 ; PMID:26619011

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713907T>A , CM000663.2:g.114713907T>A	GRCh38
NC_000001.10:g.115256528T>A , CM000663.1:g.115256528T>A	GRCh37
NC_000001.9:g.115058051T>A	NCBI36
NG_007572.1:g.7988A>T , LRG_92:g.7988A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369535.5:c.183A>T MANE Select	ENSP00000358548.4:p.Gln61His
ENST00000369535.4:c.183A>T	ENSP00000358548.4:p.Gln61His
NM_002524.4:c.183A>T	NP_002515.1:p.Gln61His
NM_002524.5:c.183A>T MANE Select	NP_002515.1:p.Gln61His