Canonical Allele Identifier: CA2570602490
Gene: NRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705141C>G , CM000663.2:g.114705141C>G GRCh38
NC_000001.10:g.115247762C>G , CM000663.1:g.115247762C>G GRCh37
NC_000001.9:g.115049285C>G NCBI36
NG_007572.1:g.16754G>C , LRG_92:g.16754G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*2953G>C MANE Select ENSP00000358548.4:n.*2953G>C
ENST00000369535.4:c.*2953G>C ENSP00000358548.4:n.*2953G>C
NM_002524.4:c.*2953G>C NP_002515.1:n.*2953G>C
NM_002524.5:c.*2953G>C MANE Select NP_002515.1:n.*2953G>C
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