Canonical Allele Identifier: CA16602361

Gene: NRAS

Linked Data

• ClinVar Variation Id: 375874
• ClinVar RCV Id: RCV000418220 ; RCV000418396 ; RCV000422640 ; RCV000423898 ; RCV000424084 ; RCV000426122 ; RCV000428055 ; RCV000429082 ; RCV000431333 ; RCV000433349 ; RCV000433761 ; RCV000435412 ; RCV000435905 ; RCV000436539 ; RCV000438738 ; RCV000441171 ; RCV000444188 ; RCV000444754 ; RCV000444899 ; RCV002524687
• dbSNP Id: rs11554290
• COSMIC: COSM583
• MyVariant Identifiers: chr1:g.115256529T>A (hg19) ; chr1:g.114713908T>A (hg38)
• CIViC: CA16602361
• PubMed: PMID:2674680 ; PMID:8120410 ; PMID:12460918 ; PMID:16291983 ; PMID:18390968 ; PMID:18948947 ; PMID:20130576 ; PMID:20149136 ; PMID:20179705 ; PMID:20406486 ; PMID:21576590 ; PMID:22761467 ; PMID:23414587 ; PMID:23515407 ; PMID:23538902 ; PMID:23569304 ; PMID:23614898 ; PMID:25157968 ; PMID:26619011

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713908T>A , CM000663.2:g.114713908T>A	GRCh38
NC_000001.10:g.115256529T>A , CM000663.1:g.115256529T>A	GRCh37
NC_000001.9:g.115058052T>A	NCBI36
NG_007572.1:g.7987A>T , LRG_92:g.7987A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369535.5:c.182A>T MANE Select	ENSP00000358548.4:p.Gln61Leu
ENST00000369535.4:c.182A>T	ENSP00000358548.4:p.Gln61Leu
NM_002524.4:c.182A>T	NP_002515.1:p.Gln61Leu
NM_002524.5:c.182A>T MANE Select	NP_002515.1:p.Gln61Leu