Canonical Allele Identifier: CA261525

Gene: NRAS

Linked Data

• ClinVar Variation Id: 40470
• ClinVar RCV Id: RCV000037576 ; RCV000158986 ; RCV000421072 ; RCV000423890 ; RCV000432178 ; RCV000419124 ; RCV000429393 ; RCV000438750 ; RCV000438967 ; RCV000439421 ; RCV001377735
• dbSNP Id: rs121913237
• gnomAD v2: 1-115258747-C-A
• gnomAD v4: 1-114716126-C-A
• COSMIC: COSM566
• MyVariant Identifiers: chr1:g.115258747C>A (hg19) ; chr1:g.114716126C>A (hg38)
• CIViC: CA261525
• PubMed: PMID:2674680 ; PMID:8120410 ; PMID:14982869 ; PMID:15046639 ; PMID:15831708 ; PMID:16273091 ; PMID:16291983 ; PMID:17699718 ; PMID:18390968 ; PMID:18952898 ; PMID:19657110 ; PMID:20130576 ; PMID:20179705 ; PMID:20619739 ; PMID:20736745 ; PMID:21305640 ; PMID:21729679 ; PMID:21829508 ; PMID:23414587 ; PMID:25157968 ; PMID:26619011

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114716126C>A , CM000663.2:g.114716126C>A	GRCh38
NC_000001.10:g.115258747C>A , CM000663.1:g.115258747C>A	GRCh37
NC_000001.9:g.115060270C>A	NCBI36
NG_007572.1:g.5769G>T , LRG_92:g.5769G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.35G>T MANE Select	ENSP00000358548.4:p.Gly12Val
ENST00000369535.4:c.35G>T	ENSP00000358548.4:p.Gly12Val
NM_002524.4:c.35G>T	NP_002515.1:p.Gly12Val
NM_002524.5:c.35G>T MANE Select	NP_002515.1:p.Gly12Val