Canonical Allele Identifier: CA29042223
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs869080813
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709556del , CM000663.2:g.114709556del GRCh38
NC_000001.10:g.115252177del , CM000663.1:g.115252177del GRCh37
NC_000001.9:g.115053700del NCBI36
NG_007572.1:g.12341del , LRG_92:g.12341del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.450+15del MANE Select ENSP00000358548.4:n.450+15del
ENST00000369535.4:c.450+15del ENSP00000358548.4:n.450+15del
NM_002524.4:c.450+15del NP_002515.1:n.450+15del
NM_002524.5:c.450+15del MANE Select NP_002515.1:n.450+15del
Search 100 bp 5'
Search 100 bp 3'