Canonical Allele Identifier: CA130423

Gene: NRAS

Linked Data

• ClinVar Variation Id: 39647
• ClinVar RCV Id: RCV000032848 ; RCV000208568
• dbSNP Id: rs397514553
• COSMIC: COSM3471679
• MyVariant Identifiers: chr1:g.115258681G>A (hg19) ; chr1:g.114716060G>A (hg38)
• PubMed: PMID:20301303 ; PMID:22499344

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114716060G>A , CM000663.2:g.114716060G>A	GRCh38
NC_000001.10:g.115258681G>A , CM000663.1:g.115258681G>A	GRCh37
NC_000001.9:g.115060204G>A	NCBI36
NG_007572.1:g.5835C>T , LRG_92:g.5835C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.101C>T MANE Select	ENSP00000358548.4:p.Pro34Leu
ENST00000369535.4:c.101C>T	ENSP00000358548.4:p.Pro34Leu
NM_002524.4:c.101C>T	NP_002515.1:p.Pro34Leu
NM_002524.5:c.101C>T MANE Select	NP_002515.1:p.Pro34Leu