Canonical Allele Identifier: CA1020747
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs114636410

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713836T>C , CM000663.2:g.114713836T>C GRCh38
NC_000001.10:g.115256457T>C , CM000663.1:g.115256457T>C GRCh37
NC_000001.9:g.115057980T>C NCBI36
NG_007572.1:g.8059A>G , LRG_92:g.8059A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.254A>G MANE Select ENSP00000358548.4:p.Asn85Ser
ENST00000369535.4:c.254A>G ENSP00000358548.4:p.Asn85Ser
NM_002524.4:c.254A>G NP_002515.1:p.Asn85Ser
NM_002524.5:c.254A>G MANE Select NP_002515.1:p.Asn85Ser