Canonical Allele Identifier: CA341741687
Gene: NRAS HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.115256556A>C (hg19) chr1:g.114713935A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713935A>C , CM000663.2:g.114713935A>C GRCh38
NC_000001.10:g.115256556A>C , CM000663.1:g.115256556A>C GRCh37
NC_000001.9:g.115058079A>C NCBI36
NG_007572.1:g.7960T>G , LRG_92:g.7960T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.155T>G MANE Select ENSP00000358548.4:p.Leu52Trp
ENST00000369535.4:c.155T>G ENSP00000358548.4:p.Leu52Trp
NM_002524.4:c.155T>G NP_002515.1:p.Leu52Trp
NM_002524.5:c.155T>G MANE Select NP_002515.1:p.Leu52Trp
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