Canonical Allele Identifier: CA341741677

Gene: NRAS

Linked Data

• dbSNP Id: rs114668710
• MyVariant Identifiers: chr1:g.115256552C>G (hg19) ; chr1:g.114713931C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713931C>G , CM000663.2:g.114713931C>G	GRCh38
NC_000001.10:g.115256552C>G , CM000663.1:g.115256552C>G	GRCh37
NC_000001.9:g.115058075C>G	NCBI36
NG_007572.1:g.7964G>C , LRG_92:g.7964G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.159G>C MANE Select	ENSP00000358548.4:p.Leu53Phe
ENST00000369535.4:c.159G>C	ENSP00000358548.4:p.Leu53Phe
NM_002524.4:c.159G>C	NP_002515.1:p.Leu53Phe
NM_002524.5:c.159G>C MANE Select	NP_002515.1:p.Leu53Phe