Canonical Allele Identifier: CA1190285666
Gene: NRAS HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707059A= , CM000663.2:g.114707059A= GRCh38
NC_000001.10:g.115249680A= , CM000663.1:g.115249680A= GRCh37
NC_000001.9:g.115051203A= NCBI36
NG_007572.1:g.14836T= , LRG_92:g.14836T=

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*1035T= MANE Select ENSP00000358548.4:n.*1035T=
ENST00000369535.4:c.*1035T= ENSP00000358548.4:n.*1035T=
NM_002524.4:c.*1035T= NP_002515.1:n.*1035T=
NM_002524.5:c.*1035T= MANE Select NP_002515.1:n.*1035T=
Search 100 bp 5'
Search 100 bp 3'