Canonical Allele Identifier: CA891841769
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713909_114713910delinsTC , CM000663.2:g.114713909_114713910delinsTC GRCh38
NC_000001.10:g.115256530_115256531delinsTC , CM000663.1:g.115256530_115256531delinsTC GRCh37
NC_000001.9:g.115058053_115058054delinsTC NCBI36
NG_007572.1:g.7985_7986delinsGA , LRG_92:g.7985_7986delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.180_181delinsGA MANE Select ENSP00000358548.4:p.Gln61Lys
ENST00000369535.4:c.180_181delinsGA ENSP00000358548.4:p.Gln61Lys
NM_002524.4:c.180_181delinsGA NP_002515.1:p.Gln61Lys
NM_002524.5:c.180_181delinsGA MANE Select NP_002515.1:p.Gln61Lys