Canonical Allele Identifier: CA1190284794

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114705879_114705880delinsCT , CM000663.2:g.114705879_114705880delinsCT	GRCh38
NC_000001.10:g.115248500_115248501delinsCT , CM000663.1:g.115248500_115248501delinsCT	GRCh37
NC_000001.9:g.115050023_115050024delinsCT	NCBI36
NG_007572.1:g.16015_16016delinsAG , LRG_92:g.16015_16016delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.*2214_*2215delinsAG MANE Select	ENSP00000358548.4:n.*2214_*2215delinsAG
ENST00000369535.4:c.*2214_*2215delinsAG	ENSP00000358548.4:n.*2214_*2215delinsAG
NM_002524.4:c.*2214_*2215delinsAG	NP_002515.1:n.*2214_*2215delinsAG
NM_002524.5:c.*2214_*2215delinsAG MANE Select	NP_002515.1:n.*2214_*2215delinsAG