Canonical Allele Identifier: CA2573050668
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713901_114713909dup , CM000663.2:g.114713901_114713909dup GRCh38
NC_000001.10:g.115256522_115256530dup , CM000663.1:g.115256522_115256530dup GRCh37
NC_000001.9:g.115058045_115058053dup NCBI36
NG_007572.1:g.7986_7994dup , LRG_92:g.7986_7994dup

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.181_189dup MANE Select ENSP00000358548.4:p.Glu63_Tyr64insGlnGluG...
ENST00000369535.4:c.181_189dup ENSP00000358548.4:p.Glu63_Tyr64insGlnGluG...
NM_002524.4:c.181_189dup NP_002515.1:p.Glu63_Tyr64insGlnGluGlu
NM_002524.5:c.181_189dup MANE Select NP_002515.1:p.Glu63_Tyr64insGlnGluGlu