Canonical Allele Identifier: CA645537984
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713882_114713888del , CM000663.2:g.114713882_114713888del GRCh38
NC_000001.10:g.115256503_115256509del , CM000663.1:g.115256503_115256509del GRCh37
NC_000001.9:g.115058026_115058032del NCBI36
NG_007572.1:g.8008_8014del , LRG_92:g.8008_8014del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.203_209del MANE Select ENSP00000358548.4:p.Arg68AsnfsTer3
ENST00000369535.4:c.203_209del ENSP00000358548.4:p.Arg68AsnfsTer3
NM_002524.4:c.203_209del NP_002515.1:p.Arg68AsnfsTer3
NM_002524.5:c.203_209del MANE Select NP_002515.1:p.Arg68AsnfsTer3