Canonical Allele Identifier: CA341739322
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101738768
COSMIC: COSM894238

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709630G>T , CM000663.2:g.114709630G>T GRCh38
NC_000001.10:g.115252251G>T , CM000663.1:g.115252251G>T GRCh37
NC_000001.9:g.115053774G>T NCBI36
NG_007572.1:g.12265C>A , LRG_92:g.12265C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.389C>A MANE Select ENSP00000358548.4:p.Ala130Asp
ENST00000369535.4:c.389C>A ENSP00000358548.4:p.Ala130Asp
NM_002524.4:c.389C>A NP_002515.1:p.Ala130Asp
NM_002524.5:c.389C>A MANE Select NP_002515.1:p.Ala130Asp