Canonical Allele Identifier: CA1190285748
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707204T= , CM000663.2:g.114707204T= GRCh38
NC_000001.10:g.115249825T= , CM000663.1:g.115249825T= GRCh37
NC_000001.9:g.115051348T= NCBI36
NG_007572.1:g.14691A= , LRG_92:g.14691A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*890A= MANE Select ENSP00000358548.4:n.*890A=
ENST00000369535.4:c.*890A= ENSP00000358548.4:n.*890A=
NM_002524.4:c.*890A= NP_002515.1:n.*890A=
NM_002524.5:c.*890A= MANE Select NP_002515.1:n.*890A=