Canonical Allele Identifier: CA1190285414
Gene: NRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114706739_114706754delinsAGTTACTGGTGCAATG , CM000663.2:g.114706739_114706754delinsAGTTACTGGTGCAATG GRCh38
NC_000001.10:g.115249360_115249375delinsAGTTACTGGTGCAATG , CM000663.1:g.115249360_115249375delinsAGTTACTGGTGCAATG GRCh37
NC_000001.9:g.115050883_115050898delinsAGTTACTGGTGCAATG NCBI36
NG_007572.1:g.15141_15156delinsCATTGCACCAGTAACT , LRG_92:g.15141_15156delinsCATTGCACCAGTAACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*1340_*1355delinsCATTGCACCAGTAACT MANE Select ENSP00000358548.4:n.*1340_*1355delinsCATTGCACCAGTAACT
ENST00000369535.4:c.*1340_*1355delinsCATTGCACCAGTAACT ENSP00000358548.4:n.*1340_*1355delinsCATTGCACCAGTAACT
NM_002524.4:c.*1340_*1355delinsCATTGCACCAGTAACT NP_002515.1:n.*1340_*1355delinsCATTGCACCAGTAACT
NM_002524.5:c.*1340_*1355delinsCATTGCACCAGTAACT MANE Select NP_002515.1:n.*1340_*1355delinsCATTGCACCAGTAACT
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