Canonical Allele Identifier: CA2579753933
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713906_114713908del , CM000663.2:g.114713906_114713908del GRCh38
NC_000001.10:g.115256527_115256529del , CM000663.1:g.115256527_115256529del GRCh37
NC_000001.9:g.115058050_115058052del NCBI36
NG_007572.1:g.7991_7993del , LRG_92:g.7991_7993del

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.186_188del MANE Select ENSP00000358548.4:p.Glu63del
ENST00000369535.4:c.186_188del ENSP00000358548.4:p.Glu63del
NM_002524.4:c.186_188del NP_002515.1:p.Glu63del
NM_002524.5:c.186_188del MANE Select NP_002515.1:p.Glu63del