Canonical Allele Identifier: CA645537981
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709735del , CM000663.2:g.114709735del GRCh38
NC_000001.10:g.115252356del , CM000663.1:g.115252356del GRCh37
NC_000001.9:g.115053879del NCBI36
NG_007572.1:g.12164del , LRG_92:g.12164del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.291-3del MANE Select ENSP00000358548.4:n.291-3del
ENST00000369535.4:c.291-3del ENSP00000358548.4:n.291-3del
NM_002524.4:c.291-3del NP_002515.1:n.291-3del
NM_002524.5:c.291-3del MANE Select NP_002515.1:n.291-3del