Canonical Allele Identifier: CA2647250701
Gene: NRAS HGNC NCBI

Linked Data

gnomAD v4: 1-114706918-GCAATTATATACATCATTAA-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114706919_114706937del , CM000663.2:g.114706919_114706937del GRCh38
NC_000001.10:g.115249540_115249558del , CM000663.1:g.115249540_115249558del GRCh37
NC_000001.9:g.115051063_115051081del NCBI36
NG_007572.1:g.14958_14976del , LRG_92:g.14958_14976del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*1157_*1175del MANE Select ENSP00000358548.4:n.*1157_*1175del
ENST00000369535.4:c.*1157_*1175del ENSP00000358548.4:n.*1157_*1175del
NM_002524.4:c.*1157_*1175del NP_002515.1:n.*1157_*1175del
NM_002524.5:c.*1157_*1175del MANE Select NP_002515.1:n.*1157_*1175del
Search 100 bp 5'
Search 100 bp 3'