Canonical Allele Identifier: CA2647248265
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713749del , CM000663.2:g.114713749del GRCh38
NC_000001.10:g.115256370del , CM000663.1:g.115256370del GRCh37
NC_000001.9:g.115057893del NCBI36
NG_007572.1:g.8148del , LRG_92:g.8148del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.290+53del MANE Select ENSP00000358548.4:n.290+53del
ENST00000369535.4:c.290+53del ENSP00000358548.4:n.290+53del
NM_002524.4:c.290+53del NP_002515.1:n.290+53del
NM_002524.5:c.290+53del MANE Select NP_002515.1:n.290+53del