Canonical Allele Identifier: CA2647253044
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709457del , CM000663.2:g.114709457del GRCh38
NC_000001.10:g.115252078del , CM000663.1:g.115252078del GRCh37
NC_000001.9:g.115053601del NCBI36
NG_007572.1:g.12444del , LRG_92:g.12444del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.450+118del MANE Select ENSP00000358548.4:n.450+118del
ENST00000369535.4:c.450+118del ENSP00000358548.4:n.450+118del
NM_002524.4:c.450+118del NP_002515.1:n.450+118del
NM_002524.5:c.450+118del MANE Select NP_002515.1:n.450+118del