Canonical Allele Identifier: CA1190285637
Gene: NRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707030_114707032delinsCAA , CM000663.2:g.114707030_114707032delinsCAA GRCh38
NC_000001.10:g.115249651_115249653delinsCAA , CM000663.1:g.115249651_115249653delinsCAA GRCh37
NC_000001.9:g.115051174_115051176delinsCAA NCBI36
NG_007572.1:g.14863_14865delinsTTG , LRG_92:g.14863_14865delinsTTG

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*1062_*1064delinsTTG MANE Select ENSP00000358548.4:n.*1062_*1064delinsTTG
ENST00000369535.4:c.*1062_*1064delinsTTG ENSP00000358548.4:n.*1062_*1064delinsTTG
NM_002524.4:c.*1062_*1064delinsTTG NP_002515.1:n.*1062_*1064delinsTTG
NM_002524.5:c.*1062_*1064delinsTTG MANE Select NP_002515.1:n.*1062_*1064delinsTTG
Search 100 bp 5'
Search 100 bp 3'