Canonical Allele Identifier: CA341741677
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs114668710

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