Canonical Allele Identifier: CA2574035358
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709580del , CM000663.2:g.114709580del GRCh38
NC_000001.10:g.115252201del , CM000663.1:g.115252201del GRCh37
NC_000001.9:g.115053724del NCBI36
NG_007572.1:g.12316del , LRG_92:g.12316del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.440del MANE Select ENSP00000358548.4:p.Lys147ArgfsTer14
ENST00000369535.4:c.440del ENSP00000358548.4:p.Lys147ArgfsTer14
NM_002524.4:c.440del NP_002515.1:p.Lys147ArgfsTer14
NM_002524.5:c.440del MANE Select NP_002515.1:p.Lys147ArgfsTer14