Canonical Allele Identifier: CA1190286056
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs933820862
gnomAD v4: 1-114707684-GAA-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707693_114707694del , CM000663.2:g.114707693_114707694del GRCh38
NC_000001.10:g.115250314_115250315del , CM000663.1:g.115250314_115250315del GRCh37
NC_000001.9:g.115051837_115051838del NCBI36
NG_007572.1:g.14209_14210del , LRG_92:g.14209_14210del

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*408_*409del MANE Select ENSP00000358548.4:n.*408_*409del
ENST00000369535.4:c.*408_*409del ENSP00000358548.4:n.*408_*409del
NM_002524.4:c.*408_*409del NP_002515.1:n.*408_*409del
NM_002524.5:c.*408_*409del MANE Select NP_002515.1:n.*408_*409del
Search 100 bp 5'
Search 100 bp 3'