Canonical Allele Identifier: CA1190285680

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114707086_114707087delinsAT , CM000663.2:g.114707086_114707087delinsAT	GRCh38
NC_000001.10:g.115249707_115249708delinsAT , CM000663.1:g.115249707_115249708delinsAT	GRCh37
NC_000001.9:g.115051230_115051231delinsAT	NCBI36
NG_007572.1:g.14808_14809delinsAT , LRG_92:g.14808_14809delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000369535.5:c.*1007_*1008delinsAT MANE Select	ENSP00000358548.4:n.*1007_*1008delinsAT
ENST00000369535.4:c.*1007_*1008delinsAT	ENSP00000358548.4:n.*1007_*1008delinsAT
NM_002524.4:c.*1007_*1008delinsAT	NP_002515.1:n.*1007_*1008delinsAT
NM_002524.5:c.*1007_*1008delinsAT MANE Select	NP_002515.1:n.*1007_*1008delinsAT