Canonical Allele Identifier: CA1190291217
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713592A= , CM000663.2:g.114713592A= GRCh38
NC_000001.10:g.115256213A= , CM000663.1:g.115256213A= GRCh37
NC_000001.9:g.115057736A= NCBI36
NG_007572.1:g.8303T= , LRG_92:g.8303T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.290+208T= MANE Select ENSP00000358548.4:n.290+208T=
ENST00000369535.4:c.290+208T= ENSP00000358548.4:n.290+208T=
NM_002524.4:c.290+208T= NP_002515.1:n.290+208T=
NM_002524.5:c.290+208T= MANE Select NP_002515.1:n.290+208T=