Canonical Allele Identifier: CA916267725
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1570867335
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705144_114705145del , CM000663.2:g.114705144_114705145del GRCh38
NC_000001.10:g.115247765_115247766del , CM000663.1:g.115247765_115247766del GRCh37
NC_000001.9:g.115049288_115049289del NCBI36
NG_007572.1:g.16752_16753del , LRG_92:g.16752_16753del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*2951_*2952del MANE Select ENSP00000358548.4:n.*2951_*2952del
ENST00000369535.4:c.*2951_*2952del ENSP00000358548.4:n.*2951_*2952del
NM_002524.4:c.*2951_*2952del NP_002515.1:n.*2951_*2952del
NM_002524.5:c.*2951_*2952del MANE Select NP_002515.1:n.*2951_*2952del
Search 100 bp 5'
Search 100 bp 3'