Canonical Allele Identifier: CA1148558966
Gene: NRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709649T= , CM000663.2:g.114709649T= GRCh38
NC_000001.10:g.115252270T= , CM000663.1:g.115252270T= GRCh37
NC_000001.9:g.115053793T= NCBI36
NG_007572.1:g.12246A= , LRG_92:g.12246A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.370A= MANE Select ENSP00000358548.4:p.Thr124=
ENST00000369535.4:c.370A= ENSP00000358548.4:p.Thr124=
NM_002524.4:c.370A= NP_002515.1:p.Thr124=
NM_002524.5:c.370A= MANE Select NP_002515.1:p.Thr124=
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