Canonical Allele Identifier: CA645537990
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713908del , CM000663.2:g.114713908del GRCh38
NC_000001.10:g.115256529del , CM000663.1:g.115256529del GRCh37
NC_000001.9:g.115058052del NCBI36
NG_007572.1:g.7988del , LRG_92:g.7988del

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.183del MANE Select ENSP00000358548.4:p.Glu62LysfsTer6
ENST00000369535.4:c.183del ENSP00000358548.4:p.Glu62LysfsTer6
NM_002524.4:c.183del NP_002515.1:p.Glu62LysfsTer6
NM_002524.5:c.183del MANE Select NP_002515.1:p.Glu62LysfsTer6