Canonical Allele Identifier: CA1190291343
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114714010G= , CM000663.2:g.114714010G= GRCh38
NC_000001.10:g.115256631G= , CM000663.1:g.115256631G= GRCh37
NC_000001.9:g.115058154G= NCBI36
NG_007572.1:g.7885C= , LRG_92:g.7885C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.112-32C= MANE Select ENSP00000358548.4:n.112-32C=
ENST00000369535.4:c.112-32C= ENSP00000358548.4:n.112-32C=
NM_002524.4:c.112-32C= NP_002515.1:n.112-32C=
NM_002524.5:c.112-32C= MANE Select NP_002515.1:n.112-32C=