Canonical Allele Identifier: CA1190291312
Gene: NRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713933A= , CM000663.2:g.114713933A= GRCh38
NC_000001.10:g.115256554A= , CM000663.1:g.115256554A= GRCh37
NC_000001.9:g.115058077A= NCBI36
NG_007572.1:g.7962T= , LRG_92:g.7962T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.157T= MANE Select ENSP00000358548.4:p.Leu53=
ENST00000369535.4:c.157T= ENSP00000358548.4:p.Leu53=
NM_002524.4:c.157T= NP_002515.1:p.Leu53=
NM_002524.5:c.157T= MANE Select NP_002515.1:p.Leu53=
Search 100 bp 5'
Search 100 bp 3'