Canonical Allele Identifier: CA1190289022
Gene: NRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114708129G= , CM000663.2:g.114708129G= GRCh38
NC_000001.10:g.115250750G= , CM000663.1:g.115250750G= GRCh37
NC_000001.9:g.115052273G= NCBI36
NG_007572.1:g.13766C= , LRG_92:g.13766C=

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*43+25C= MANE Select ENSP00000358548.4:n.*43+25C=
ENST00000369535.4:c.*43+25C= ENSP00000358548.4:n.*43+25C=
NM_002524.4:c.*43+25C= NP_002515.1:n.*43+25C=
NM_002524.5:c.*43+25C= MANE Select NP_002515.1:n.*43+25C=
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