Canonical Allele Identifier: CA1143538228
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713941G= , CM000663.2:g.114713941G= GRCh38
NC_000001.10:g.115256562G= , CM000663.1:g.115256562G= GRCh37
NC_000001.9:g.115058085G= NCBI36
NG_007572.1:g.7954C= , LRG_92:g.7954C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.149C= MANE Select ENSP00000358548.4:p.Thr50=
ENST00000369535.4:c.149C= ENSP00000358548.4:p.Thr50=
NM_002524.4:c.149C= NP_002515.1:p.Thr50=
NM_002524.5:c.149C= MANE Select NP_002515.1:p.Thr50=