Canonical Allele Identifier: CA341739141
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1658995926

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709598A>T , CM000663.2:g.114709598A>T GRCh38
NC_000001.10:g.115252219A>T , CM000663.1:g.115252219A>T GRCh37
NC_000001.9:g.115053742A>T NCBI36
NG_007572.1:g.12297T>A , LRG_92:g.12297T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.421T>A MANE Select ENSP00000358548.4:p.Phe141Ile
ENST00000369535.4:c.421T>A ENSP00000358548.4:p.Phe141Ile
NM_002524.4:c.421T>A NP_002515.1:p.Phe141Ile
NM_002524.5:c.421T>A MANE Select NP_002515.1:p.Phe141Ile