Canonical Allele Identifier: CA645537986
Gene: NRAS HGNC NCBI

Linked Data

COSMIC: COSM5878735
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713895_114713896delinsTTGCTGTA , CM000663.2:g.114713895_114713896delinsTTGCTGTA GRCh38
NC_000001.10:g.115256516_115256517delinsTTGCTGTA , CM000663.1:g.115256516_115256517delinsTTGCTGTA GRCh37
NC_000001.9:g.115058039_115058040delinsTTGCTGTA NCBI36
NG_007572.1:g.7999_8000delinsTACAGCAA , LRG_92:g.7999_8000delinsTACAGCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.194_195delinsTACAGCAA MANE Select ENSP00000358548.4:p.Ser65delinsIleGlnGln
ENST00000369535.4:c.194_195delinsTACAGCAA ENSP00000358548.4:p.Ser65delinsIleGlnGln
NM_002524.4:c.194_195delinsTACAGCAA NP_002515.1:p.Ser65delinsIleGlnGln
NM_002524.5:c.194_195delinsTACAGCAA MANE Select NP_002515.1:p.Ser65delinsIleGlnGln
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Search 100 bp 3'