Canonical Allele Identifier: CA2647248246
Gene: NRAS HGNC NCBI

Linked Data

gnomAD v4: 1-114713716-CTTCCCTAGTG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713718_114713727del , CM000663.2:g.114713718_114713727del GRCh38
NC_000001.10:g.115256339_115256348del , CM000663.1:g.115256339_115256348del GRCh37
NC_000001.9:g.115057862_115057871del NCBI36
NG_007572.1:g.8169_8178del , LRG_92:g.8169_8178del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.290+74_290+83del MANE Select ENSP00000358548.4:n.290+74_290+83del
ENST00000369535.4:c.290+74_290+83del ENSP00000358548.4:n.290+74_290+83del
NM_002524.4:c.290+74_290+83del NP_002515.1:n.290+74_290+83del
NM_002524.5:c.290+74_290+83del MANE Select NP_002515.1:n.290+74_290+83del
Search 100 bp 5'
Search 100 bp 3'