Canonical Allele Identifier: CA341741249
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713775_114713779del , CM000663.2:g.114713775_114713779del GRCh38
NC_000001.10:g.115256396_115256400del , CM000663.1:g.115256396_115256400del GRCh37
NC_000001.9:g.115057919_115057923del NCBI36
NG_007572.1:g.8116_8120del , LRG_92:g.8116_8120del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.290+21_290+25del MANE Select ENSP00000358548.4:n.290+21_290+25del
ENST00000369535.4:c.290+21_290+25del ENSP00000358548.4:n.290+21_290+25del
NM_002524.4:c.290+21_290+25del NP_002515.1:n.290+21_290+25del
NM_002524.5:c.290+21_290+25del MANE Select NP_002515.1:n.290+21_290+25del