Canonical Allele Identifier: CA341741351
Gene: NRAS HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.115256442A>T (hg19) chr1:g.114713821A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713821A>T , CM000663.2:g.114713821A>T GRCh38
NC_000001.10:g.115256442A>T , CM000663.1:g.115256442A>T GRCh37
NC_000001.9:g.115057965A>T NCBI36
NG_007572.1:g.8074T>A , LRG_92:g.8074T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.269T>A MANE Select ENSP00000358548.4:p.Phe90Tyr
ENST00000369535.4:c.269T>A ENSP00000358548.4:p.Phe90Tyr
NM_002524.4:c.269T>A NP_002515.1:p.Phe90Tyr
NM_002524.5:c.269T>A MANE Select NP_002515.1:p.Phe90Tyr
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