Canonical Allele Identifier: CA10602732

Gene: NRAS

Linked Data

• ClinVar Variation Id: 280409
• ClinVar RCV Id: RCV000291285 ; RCV000426654 ; RCV000428903 ; RCV000430000 ; RCV000421496 ; RCV000432170 ; RCV000427746 ; RCV000431592 ; RCV000437545 ; RCV000439526 ; RCV000439765 ; RCV000444660 ; RCV000419053 ; RCV000419201 ; RCV000421291 ; RCV000434604 ; RCV000444278 ; RCV000420302 ; RCV000437312 ; RCV000438468 ; RCV003155143
• dbSNP Id: rs11554290
• MyVariant Identifiers: chr1:g.115256529T>G (hg19) ; chr1:g.114713908T>G (hg38)
• PubMed: PMID:2674680 ; PMID:8120410 ; PMID:16291983 ; PMID:18390968 ; PMID:20130576 ; PMID:20179705 ; PMID:22761467 ; PMID:23414587 ; PMID:23538902 ; PMID:23569304 ; PMID:23614898 ; PMID:24370118 ; PMID:25157968 ; PMID:26619011

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.182A>C MANE Select	ENSP00000358548.4:p.Gln61Pro
ENST00000369535.4:c.182A>C	ENSP00000358548.4:p.Gln61Pro
NM_002524.4:c.182A>C	NP_002515.1:p.Gln61Pro
NM_002524.5:c.182A>C MANE Select	NP_002515.1:p.Gln61Pro