Canonical Allele Identifier: CA1190289504
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709702G= , CM000663.2:g.114709702G= GRCh38
NC_000001.10:g.115252323G= , CM000663.1:g.115252323G= GRCh37
NC_000001.9:g.115053846G= NCBI36
NG_007572.1:g.12193C= , LRG_92:g.12193C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.317C= MANE Select ENSP00000358548.4:p.Ser106=
ENST00000369535.4:c.317C= ENSP00000358548.4:p.Ser106=
NM_002524.4:c.317C= NP_002515.1:p.Ser106=
NM_002524.5:c.317C= MANE Select NP_002515.1:p.Ser106=