Canonical Allele Identifier: CA1190284276

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114705170_114705171delinsCT , CM000663.2:g.114705170_114705171delinsCT	GRCh38
NC_000001.10:g.115247791_115247792delinsCT , CM000663.1:g.115247791_115247792delinsCT	GRCh37
NC_000001.9:g.115049314_115049315delinsCT	NCBI36
NG_007572.1:g.16724_16725delinsAG , LRG_92:g.16724_16725delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000369535.5:c.*2923_*2924delinsAG MANE Select	ENSP00000358548.4:n.*2923_*2924delinsAG
ENST00000369535.4:c.*2923_*2924delinsAG	ENSP00000358548.4:n.*2923_*2924delinsAG
NM_002524.4:c.*2923_*2924delinsAG	NP_002515.1:n.*2923_*2924delinsAG
NM_002524.5:c.*2923_*2924delinsAG MANE Select	NP_002515.1:n.*2923_*2924delinsAG