Canonical Allele Identifier: CA2695202599
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713911_114713913del , CM000663.2:g.114713911_114713913del GRCh38
NC_000001.10:g.115256532_115256534del , CM000663.1:g.115256532_115256534del GRCh37
NC_000001.9:g.115058055_115058057del NCBI36
NG_007572.1:g.7982_7984del , LRG_92:g.7982_7984del

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.177_179del MANE Select ENSP00000358548.4:p.Gly60del
ENST00000369535.4:c.177_179del ENSP00000358548.4:p.Gly60del
NM_002524.4:c.177_179del NP_002515.1:p.Gly60del
NM_002524.5:c.177_179del MANE Select NP_002515.1:p.Gly60del