Canonical Allele Identifier: CA1190291331
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713992G= , CM000663.2:g.114713992G= GRCh38
NC_000001.10:g.115256613G= , CM000663.1:g.115256613G= GRCh37
NC_000001.9:g.115058136G= NCBI36
NG_007572.1:g.7903C= , LRG_92:g.7903C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.112-14C= MANE Select ENSP00000358548.4:n.112-14C=
ENST00000369535.4:c.112-14C= ENSP00000358548.4:n.112-14C=
NM_002524.4:c.112-14C= NP_002515.1:n.112-14C=
NM_002524.5:c.112-14C= MANE Select NP_002515.1:n.112-14C=