Canonical Allele Identifier: CA1145905805
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705579_114705587delinsTAACTATAA , CM000663.2:g.114705579_114705587delinsTAACTATAA GRCh38
NC_000001.10:g.115248200_115248208delinsTAACTATAA , CM000663.1:g.115248200_115248208delinsTAACTATAA GRCh37
NC_000001.9:g.115049723_115049731delinsTAACTATAA NCBI36
NG_007572.1:g.16308_16316delinsTTATAGTTA , LRG_92:g.16308_16316delinsTTATAGTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*2507_*2515delinsTTATAGTTA MANE Select ENSP00000358548.4:n.*2507_*2515delinsTTATAGTTA
ENST00000369535.4:c.*2507_*2515delinsTTATAGTTA ENSP00000358548.4:n.*2507_*2515delinsTTATAGTTA
NM_002524.4:c.*2507_*2515delinsTTATAGTTA NP_002515.1:n.*2507_*2515delinsTTATAGTTA
NM_002524.5:c.*2507_*2515delinsTTATAGTTA MANE Select NP_002515.1:n.*2507_*2515delinsTTATAGTTA