Canonical Allele Identifier: CA645537988
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101742008
COSMIC: COSM26494
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713906_114713907delinsTG , CM000663.2:g.114713906_114713907delinsTG GRCh38
NC_000001.10:g.115256527_115256528delinsTG , CM000663.1:g.115256527_115256528delinsTG GRCh37
NC_000001.9:g.115058050_115058051delinsTG NCBI36
NG_007572.1:g.7988_7989delinsCA , LRG_92:g.7988_7989delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.183_184delinsCA MANE Select ENSP00000358548.4:p.Gln61_Glu62delinsHisL...
ENST00000369535.4:c.183_184delinsCA ENSP00000358548.4:p.Gln61_Glu62delinsHisL...
NM_002524.4:c.183_184delinsCA NP_002515.1:p.Gln61_Glu62delinsHisLys
NM_002524.5:c.183_184delinsCA MANE Select NP_002515.1:p.Gln61_Glu62delinsHisLys
Search 100 bp 5'
Search 100 bp 3'