Canonical Allele Identifier: CA1143833598
Gene: NRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707354C= , CM000663.2:g.114707354C= GRCh38
NC_000001.10:g.115249975C= , CM000663.1:g.115249975C= GRCh37
NC_000001.9:g.115051498C= NCBI36
NG_007572.1:g.14541G= , LRG_92:g.14541G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*740G= MANE Select ENSP00000358548.4:n.*740G=
ENST00000369535.4:c.*740G= ENSP00000358548.4:n.*740G=
NM_002524.4:c.*740G= NP_002515.1:n.*740G=
NM_002524.5:c.*740G= MANE Select NP_002515.1:n.*740G=
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