Canonical Allele Identifier: CA297023

Gene: NRAS

Linked Data

• ClinVar Variation Id: 40473
• ClinVar RCV Id: RCV000158981 ; RCV002470724 ; RCV004017274
• dbSNP Id: rs730880965
• COSMIC: COSM578
• MyVariant Identifiers: chr1:g.115256536C>T (hg19) ; chr1:g.114713915C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713915C>T , CM000663.2:g.114713915C>T	GRCh38
NC_000001.10:g.115256536C>T , CM000663.1:g.115256536C>T	GRCh37
NC_000001.9:g.115058059C>T	NCBI36
NG_007572.1:g.7980G>A , LRG_92:g.7980G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.175G>A MANE Select	ENSP00000358548.4:p.Ala59Thr
ENST00000369535.4:c.175G>A	ENSP00000358548.4:p.Ala59Thr
NM_002524.4:c.175G>A	NP_002515.1:p.Ala59Thr
NM_002524.5:c.175G>A MANE Select	NP_002515.1:p.Ala59Thr