Canonical Allele Identifier: CA1190286065
Gene: NRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707700A= , CM000663.2:g.114707700A= GRCh38
NC_000001.10:g.115250321A= , CM000663.1:g.115250321A= GRCh37
NC_000001.9:g.115051844A= NCBI36
NG_007572.1:g.14195T= , LRG_92:g.14195T=

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*394T= MANE Select ENSP00000358548.4:n.*394T=
ENST00000369535.4:c.*394T= ENSP00000358548.4:n.*394T=
NM_002524.4:c.*394T= NP_002515.1:n.*394T=
NM_002524.5:c.*394T= MANE Select NP_002515.1:n.*394T=
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