Canonical Allele Identifier: CA1190284297
Gene: NRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705236C= , CM000663.2:g.114705236C= GRCh38
NC_000001.10:g.115247857C= , CM000663.1:g.115247857C= GRCh37
NC_000001.9:g.115049380C= NCBI36
NG_007572.1:g.16659G= , LRG_92:g.16659G=

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*2858G= MANE Select ENSP00000358548.4:n.*2858G=
ENST00000369535.4:c.*2858G= ENSP00000358548.4:n.*2858G=
NM_002524.4:c.*2858G= NP_002515.1:n.*2858G=
NM_002524.5:c.*2858G= MANE Select NP_002515.1:n.*2858G=
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