Canonical Allele Identifier: CA645537985
Gene: NRAS HGNC NCBI

Linked Data

COSMIC: COSM5760827
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713893_114713894del , CM000663.2:g.114713893_114713894del GRCh38
NC_000001.10:g.115256514_115256515del , CM000663.1:g.115256514_115256515del GRCh37
NC_000001.9:g.115058037_115058038del NCBI36
NG_007572.1:g.8001_8002del , LRG_92:g.8001_8002del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.196_197del MANE Select ENSP00000358548.4:p.Ala66HisfsTer20
ENST00000369535.4:c.196_197del ENSP00000358548.4:p.Ala66HisfsTer20
NM_002524.4:c.196_197del NP_002515.1:p.Ala66HisfsTer20
NM_002524.5:c.196_197del MANE Select NP_002515.1:p.Ala66HisfsTer20
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