Canonical Allele Identifier: CA1190291309
Gene: NRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713924G= , CM000663.2:g.114713924G= GRCh38
NC_000001.10:g.115256545G= , CM000663.1:g.115256545G= GRCh37
NC_000001.9:g.115058068G= NCBI36
NG_007572.1:g.7971C= , LRG_92:g.7971C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.166C= MANE Select ENSP00000358548.4:p.Leu56=
ENST00000369535.4:c.166C= ENSP00000358548.4:p.Leu56=
NM_002524.4:c.166C= NP_002515.1:p.Leu56=
NM_002524.5:c.166C= MANE Select NP_002515.1:p.Leu56=
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