Canonical Allele Identifier: CA1190284261
Gene: NRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705141_114705143delinsCAT , CM000663.2:g.114705141_114705143delinsCAT GRCh38
NC_000001.10:g.115247762_115247764delinsCAT , CM000663.1:g.115247762_115247764delinsCAT GRCh37
NC_000001.9:g.115049285_115049287delinsCAT NCBI36
NG_007572.1:g.16752_16754delinsATG , LRG_92:g.16752_16754delinsATG

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*2951_*2953delinsATG MANE Select ENSP00000358548.4:n.*2951_*2953delinsATG
ENST00000369535.4:c.*2951_*2953delinsATG ENSP00000358548.4:n.*2951_*2953delinsATG
NM_002524.4:c.*2951_*2953delinsATG NP_002515.1:n.*2951_*2953delinsATG
NM_002524.5:c.*2951_*2953delinsATG MANE Select NP_002515.1:n.*2951_*2953delinsATG
Search 100 bp 5'
Search 100 bp 3'