Canonical Allele Identifier: CA1190284663
Gene: NRAS HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705686C= , CM000663.2:g.114705686C= GRCh38
NC_000001.10:g.115248307C= , CM000663.1:g.115248307C= GRCh37
NC_000001.9:g.115049830C= NCBI36
NG_007572.1:g.16209G= , LRG_92:g.16209G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*2408G= MANE Select ENSP00000358548.4:n.*2408G=
ENST00000369535.4:c.*2408G= ENSP00000358548.4:n.*2408G=
NM_002524.4:c.*2408G= NP_002515.1:n.*2408G=
NM_002524.5:c.*2408G= MANE Select NP_002515.1:n.*2408G=
Search 100 bp 5'
Search 100 bp 3'