Canonical Allele Identifier: CA1143538226
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713911C= , CM000663.2:g.114713911C= GRCh38
NC_000001.10:g.115256532C= , CM000663.1:g.115256532C= GRCh37
NC_000001.9:g.115058055C= NCBI36
NG_007572.1:g.7984G= , LRG_92:g.7984G=

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.179G= MANE Select ENSP00000358548.4:p.Gly60=
ENST00000369535.4:c.179G= ENSP00000358548.4:p.Gly60=
NM_002524.4:c.179G= NP_002515.1:p.Gly60=
NM_002524.5:c.179G= MANE Select NP_002515.1:p.Gly60=