Canonical Allele Identifier: CA645537994
Gene: NRAS HGNC NCBI

Linked Data

COSMIC: COSM221918

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713909_114713910delinsTG , CM000663.2:g.114713909_114713910delinsTG GRCh38
NC_000001.10:g.115256530_115256531delinsTG , CM000663.1:g.115256530_115256531delinsTG GRCh37
NC_000001.9:g.115058053_115058054delinsTG NCBI36
NG_007572.1:g.7985_7986delinsCA , LRG_92:g.7985_7986delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.180_181delinsCA MANE Select ENSP00000358548.4:p.Gln61Lys
ENST00000369535.4:c.180_181delinsCA ENSP00000358548.4:p.Gln61Lys
NM_002524.4:c.180_181delinsCA NP_002515.1:p.Gln61Lys
NM_002524.5:c.180_181delinsCA MANE Select NP_002515.1:p.Gln61Lys