Canonical Allele Identifier: CA2647248217
Gene: NRAS HGNC NCBI

Linked Data

gnomAD v4: 1-114713676-CAACCTA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713679_114713684del , CM000663.2:g.114713679_114713684del GRCh38
NC_000001.10:g.115256300_115256305del , CM000663.1:g.115256300_115256305del GRCh37
NC_000001.9:g.115057823_115057828del NCBI36
NG_007572.1:g.8213_8218del , LRG_92:g.8213_8218del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.290+118_290+123del MANE Select ENSP00000358548.4:n.290+118_290+123del
ENST00000369535.4:c.290+118_290+123del ENSP00000358548.4:n.290+118_290+123del
NM_002524.4:c.290+118_290+123del NP_002515.1:n.290+118_290+123del
NM_002524.5:c.290+118_290+123del MANE Select NP_002515.1:n.290+118_290+123del
Search 100 bp 5'
Search 100 bp 3'