Canonical Allele Identifier: CA1190284338
Gene: NRAS HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705315C= , CM000663.2:g.114705315C= GRCh38
NC_000001.10:g.115247936C= , CM000663.1:g.115247936C= GRCh37
NC_000001.9:g.115049459C= NCBI36
NG_007572.1:g.16580G= , LRG_92:g.16580G=

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*2779G= MANE Select ENSP00000358548.4:n.*2779G=
ENST00000369535.4:c.*2779G= ENSP00000358548.4:n.*2779G=
NM_002524.4:c.*2779G= NP_002515.1:n.*2779G=
NM_002524.5:c.*2779G= MANE Select NP_002515.1:n.*2779G=
Search 100 bp 5'
Search 100 bp 3'