Canonical Allele Identifier: CA1190285791
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707277C= , CM000663.2:g.114707277C= GRCh38
NC_000001.10:g.115249898C= , CM000663.1:g.115249898C= GRCh37
NC_000001.9:g.115051421C= NCBI36
NG_007572.1:g.14618G= , LRG_92:g.14618G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*817G= MANE Select ENSP00000358548.4:n.*817G=
ENST00000369535.4:c.*817G= ENSP00000358548.4:n.*817G=
NM_002524.4:c.*817G= NP_002515.1:n.*817G=
NM_002524.5:c.*817G= MANE Select NP_002515.1:n.*817G=