Canonical Allele Identifier: CA1190291251
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713709G= , CM000663.2:g.114713709G= GRCh38
NC_000001.10:g.115256330G= , CM000663.1:g.115256330G= GRCh37
NC_000001.9:g.115057853G= NCBI36
NG_007572.1:g.8186C= , LRG_92:g.8186C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.290+91C= MANE Select ENSP00000358548.4:n.290+91C=
ENST00000369535.4:c.290+91C= ENSP00000358548.4:n.290+91C=
NM_002524.4:c.290+91C= NP_002515.1:n.290+91C=
NM_002524.5:c.290+91C= MANE Select NP_002515.1:n.290+91C=