Canonical Allele Identifier: CA2745134360
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114706882del , CM000663.2:g.114706882del GRCh38
NC_000001.10:g.115249503del , CM000663.1:g.115249503del GRCh37
NC_000001.9:g.115051026del NCBI36
NG_007572.1:g.15017del , LRG_92:g.15017del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*1216del MANE Select ENSP00000358548.4:n.*1216del
ENST00000369535.4:c.*1216del ENSP00000358548.4:n.*1216del
NM_002524.4:c.*1216del NP_002515.1:n.*1216del
NM_002524.5:c.*1216del MANE Select NP_002515.1:n.*1216del