Canonical Allele Identifier: CA2537300846
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705139del , CM000663.2:g.114705139del GRCh38
NC_000001.10:g.115247760del , CM000663.1:g.115247760del GRCh37
NC_000001.9:g.115049283del NCBI36
NG_007572.1:g.16759del , LRG_92:g.16759del

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*2958del MANE Select ENSP00000358548.4:n.*2958del
ENST00000369535.4:c.*2958del ENSP00000358548.4:n.*2958del
NM_002524.4:c.*2958del NP_002515.1:n.*2958del
NM_002524.5:c.*2958del MANE Select NP_002515.1:n.*2958del