Canonical Allele Identifier: CA1190285763
Gene: NRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707228_114707230delinsTCA , CM000663.2:g.114707228_114707230delinsTCA GRCh38
NC_000001.10:g.115249849_115249851delinsTCA , CM000663.1:g.115249849_115249851delinsTCA GRCh37
NC_000001.9:g.115051372_115051374delinsTCA NCBI36
NG_007572.1:g.14665_14667delinsTGA , LRG_92:g.14665_14667delinsTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*864_*866delinsTGA MANE Select ENSP00000358548.4:n.*864_*866delinsTGA
ENST00000369535.4:c.*864_*866delinsTGA ENSP00000358548.4:n.*864_*866delinsTGA
NM_002524.4:c.*864_*866delinsTGA NP_002515.1:n.*864_*866delinsTGA
NM_002524.5:c.*864_*866delinsTGA MANE Select NP_002515.1:n.*864_*866delinsTGA
Search 100 bp 5'
Search 100 bp 3'