Canonical Allele Identifier: CA1190285745
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707198A= , CM000663.2:g.114707198A= GRCh38
NC_000001.10:g.115249819A= , CM000663.1:g.115249819A= GRCh37
NC_000001.9:g.115051342A= NCBI36
NG_007572.1:g.14697T= , LRG_92:g.14697T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*896T= MANE Select ENSP00000358548.4:n.*896T=
ENST00000369535.4:c.*896T= ENSP00000358548.4:n.*896T=
NM_002524.4:c.*896T= NP_002515.1:n.*896T=
NM_002524.5:c.*896T= MANE Select NP_002515.1:n.*896T=