Canonical Allele Identifier: CA1190289483
Gene: NRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709598A= , CM000663.2:g.114709598A= GRCh38
NC_000001.10:g.115252219A= , CM000663.1:g.115252219A= GRCh37
NC_000001.9:g.115053742A= NCBI36
NG_007572.1:g.12297T= , LRG_92:g.12297T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.421T= MANE Select ENSP00000358548.4:p.Phe141=
ENST00000369535.4:c.421T= ENSP00000358548.4:p.Phe141=
NM_002524.4:c.421T= NP_002515.1:p.Phe141=
NM_002524.5:c.421T= MANE Select NP_002515.1:p.Phe141=
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