Canonical Allele Identifier: CA341741374
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713826C>A , CM000663.2:g.114713826C>A GRCh38
NC_000001.10:g.115256447C>A , CM000663.1:g.115256447C>A GRCh37
NC_000001.9:g.115057970C>A NCBI36
NG_007572.1:g.8069G>T , LRG_92:g.8069G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.264G>T MANE Select ENSP00000358548.4:p.Lys88Asn
ENST00000369535.4:c.264G>T ENSP00000358548.4:p.Lys88Asn
NM_002524.4:c.264G>T NP_002515.1:p.Lys88Asn
NM_002524.5:c.264G>T MANE Select NP_002515.1:p.Lys88Asn