Canonical Allele Identifier: CA341741723
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101742129

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713951C>T , CM000663.2:g.114713951C>T GRCh38
NC_000001.10:g.115256572C>T , CM000663.1:g.115256572C>T GRCh37
NC_000001.9:g.115058095C>T NCBI36
NG_007572.1:g.7944G>A , LRG_92:g.7944G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.139G>A MANE Select ENSP00000358548.4:p.Asp47Asn
ENST00000369535.4:c.139G>A ENSP00000358548.4:p.Asp47Asn
NM_002524.4:c.139G>A NP_002515.1:p.Asp47Asn
NM_002524.5:c.139G>A MANE Select NP_002515.1:p.Asp47Asn