Canonical Allele Identifier: CA1190285506

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114706876_114706877delinsGT , CM000663.2:g.114706876_114706877delinsGT	GRCh38
NC_000001.10:g.115249497_115249498delinsGT , CM000663.1:g.115249497_115249498delinsGT	GRCh37
NC_000001.9:g.115051020_115051021delinsGT	NCBI36
NG_007572.1:g.15018_15019delinsAC , LRG_92:g.15018_15019delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.*1217_*1218delinsAC MANE Select	ENSP00000358548.4:n.*1217_*1218delinsAC
ENST00000369535.4:c.*1217_*1218delinsAC	ENSP00000358548.4:n.*1217_*1218delinsAC
NM_002524.4:c.*1217_*1218delinsAC	NP_002515.1:n.*1217_*1218delinsAC
NM_002524.5:c.*1217_*1218delinsAC MANE Select	NP_002515.1:n.*1217_*1218delinsAC