Canonical Allele Identifier: CA2500626894
Gene: NRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114706916_114706921del , CM000663.2:g.114706916_114706921del GRCh38
NC_000001.10:g.115249537_115249542del , CM000663.1:g.115249537_115249542del GRCh37
NC_000001.9:g.115051060_115051065del NCBI36
NG_007572.1:g.14975_14980del , LRG_92:g.14975_14980del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*1174_*1179del MANE Select ENSP00000358548.4:n.*1174_*1179del
ENST00000369535.4:c.*1174_*1179del ENSP00000358548.4:n.*1174_*1179del
NM_002524.4:c.*1174_*1179del NP_002515.1:n.*1174_*1179del
NM_002524.5:c.*1174_*1179del MANE Select NP_002515.1:n.*1174_*1179del
Search 100 bp 5'
Search 100 bp 3'