Canonical Allele Identifier: CA2696725701
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101738603
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709575_114709579del , CM000663.2:g.114709575_114709579del GRCh38
NC_000001.10:g.115252196_115252200del , CM000663.1:g.115252196_115252200del GRCh37
NC_000001.9:g.115053719_115053723del NCBI36
NG_007572.1:g.12320_12324del , LRG_92:g.12320_12324del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.444_448del MANE Select ENSP00000358548.4:p.Arg149GlyfsTer3
ENST00000369535.4:c.444_448del ENSP00000358548.4:p.Arg149GlyfsTer3
NM_002524.4:c.444_448del NP_002515.1:p.Arg149GlyfsTer3
NM_002524.5:c.444_448del MANE Select NP_002515.1:p.Arg149GlyfsTer3
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