Canonical Allele Identifier: CA10607584
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 291949
dbSNP Id: rs776606789

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705289A>G , CM000663.2:g.114705289A>G GRCh38
NC_000001.10:g.115247910A>G , CM000663.1:g.115247910A>G GRCh37
NC_000001.9:g.115049433A>G NCBI36
NG_007572.1:g.16606T>C , LRG_92:g.16606T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*2805T>C MANE Select ENSP00000358548.4:n.*2805T>C
ENST00000369535.4:c.*2805T>C ENSP00000358548.4:n.*2805T>C
NM_002524.4:c.*2805T>C NP_002515.1:n.*2805T>C
NM_002524.5:c.*2805T>C MANE Select NP_002515.1:n.*2805T>C