Canonical Allele Identifier: CA1190284316
Gene: NRAS HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705281T= , CM000663.2:g.114705281T= GRCh38
NC_000001.10:g.115247902T= , CM000663.1:g.115247902T= GRCh37
NC_000001.9:g.115049425T= NCBI36
NG_007572.1:g.16614A= , LRG_92:g.16614A=

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*2813A= MANE Select ENSP00000358548.4:n.*2813A=
ENST00000369535.4:c.*2813A= ENSP00000358548.4:n.*2813A=
NM_002524.4:c.*2813A= NP_002515.1:n.*2813A=
NM_002524.5:c.*2813A= MANE Select NP_002515.1:n.*2813A=
Search 100 bp 5'
Search 100 bp 3'