Canonical Allele Identifier: CA1190285743
Gene: NRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707194G= , CM000663.2:g.114707194G= GRCh38
NC_000001.10:g.115249815G= , CM000663.1:g.115249815G= GRCh37
NC_000001.9:g.115051338G= NCBI36
NG_007572.1:g.14701C= , LRG_92:g.14701C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*900C= MANE Select ENSP00000358548.4:n.*900C=
ENST00000369535.4:c.*900C= ENSP00000358548.4:n.*900C=
NM_002524.4:c.*900C= NP_002515.1:n.*900C=
NM_002524.5:c.*900C= MANE Select NP_002515.1:n.*900C=
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