Canonical Allele Identifier: CA1142152817
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713774_114713778delinsTTCAG , CM000663.2:g.114713774_114713778delinsTTCAG GRCh38
NC_000001.10:g.115256395_115256399delinsTTCAG , CM000663.1:g.115256395_115256399delinsTTCAG GRCh37
NC_000001.9:g.115057918_115057922delinsTTCAG NCBI36
NG_007572.1:g.8117_8121delinsCTGAA , LRG_92:g.8117_8121delinsCTGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.290+22_290+26delinsCTGAA MANE Select ENSP00000358548.4:n.290+22_290+26delinsCTGAA
ENST00000369535.4:c.290+22_290+26delinsCTGAA ENSP00000358548.4:n.290+22_290+26delinsCTGAA
NM_002524.4:c.290+22_290+26delinsCTGAA NP_002515.1:n.290+22_290+26delinsCTGAA
NM_002524.5:c.290+22_290+26delinsCTGAA MANE Select NP_002515.1:n.290+22_290+26delinsCTGAA