Canonical Allele Identifier: CA525408865
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1286183331
gnomAD v2: 1-115252059-AAAAAT-A
gnomAD v3: 1-114709438-AAAAAT-A
gnomAD v4: 1-114709438-AAAAAT-A
MyVariant Identifiers: chr1:g.115252060_115252064del (hg19) chr1:g.114709439_114709443del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709443_114709447del , CM000663.2:g.114709443_114709447del GRCh38
NC_000001.10:g.115252064_115252068del , CM000663.1:g.115252064_115252068del GRCh37
NC_000001.9:g.115053587_115053591del NCBI36
NG_007572.1:g.12452_12456del , LRG_92:g.12452_12456del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.450+126_450+130del MANE Select ENSP00000358548.4:n.450+126_450+130del
ENST00000369535.4:c.450+126_450+130del ENSP00000358548.4:n.450+126_450+130del
NM_002524.4:c.450+126_450+130del NP_002515.1:n.450+126_450+130del
NM_002524.5:c.450+126_450+130del MANE Select NP_002515.1:n.450+126_450+130del
Search 100 bp 5'
Search 100 bp 3'