Canonical Allele Identifier: CA341741669
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713928G>T , CM000663.2:g.114713928G>T GRCh38
NC_000001.10:g.115256549G>T , CM000663.1:g.115256549G>T GRCh37
NC_000001.9:g.115058072G>T NCBI36
NG_007572.1:g.7967C>A , LRG_92:g.7967C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.162C>A MANE Select ENSP00000358548.4:p.Asp54Glu
ENST00000369535.4:c.162C>A ENSP00000358548.4:p.Asp54Glu
NM_002524.4:c.162C>A NP_002515.1:p.Asp54Glu
NM_002524.5:c.162C>A MANE Select NP_002515.1:p.Asp54Glu