Canonical Allele Identifier: CA1190285861
Gene: NRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707379A= , CM000663.2:g.114707379A= GRCh38
NC_000001.10:g.115250000A= , CM000663.1:g.115250000A= GRCh37
NC_000001.9:g.115051523A= NCBI36
NG_007572.1:g.14516T= , LRG_92:g.14516T=

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*715T= MANE Select ENSP00000358548.4:n.*715T=
ENST00000369535.4:c.*715T= ENSP00000358548.4:n.*715T=
NM_002524.4:c.*715T= NP_002515.1:n.*715T=
NM_002524.5:c.*715T= MANE Select NP_002515.1:n.*715T=
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