Canonical Allele Identifier: CA341741663
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1723143
ClinVar RCV Id: RCV002306250

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713926A>G , CM000663.2:g.114713926A>G GRCh38
NC_000001.10:g.115256547A>G , CM000663.1:g.115256547A>G GRCh37
NC_000001.9:g.115058070A>G NCBI36
NG_007572.1:g.7969T>C , LRG_92:g.7969T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.164T>C MANE Select ENSP00000358548.4:p.Ile55Thr
ENST00000369535.4:c.164T>C ENSP00000358548.4:p.Ile55Thr
NM_002524.4:c.164T>C NP_002515.1:p.Ile55Thr
NM_002524.5:c.164T>C MANE Select NP_002515.1:p.Ile55Thr