Canonical Allele Identifier: CA1190291347
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114714013G= , CM000663.2:g.114714013G= GRCh38
NC_000001.10:g.115256634G= , CM000663.1:g.115256634G= GRCh37
NC_000001.9:g.115058157G= NCBI36
NG_007572.1:g.7882C= , LRG_92:g.7882C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.112-35C= MANE Select ENSP00000358548.4:n.112-35C=
ENST00000369535.4:c.112-35C= ENSP00000358548.4:n.112-35C=
NM_002524.4:c.112-35C= NP_002515.1:n.112-35C=
NM_002524.5:c.112-35C= MANE Select NP_002515.1:n.112-35C=