Canonical Allele Identifier: CA1190284840

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114705925_114705929delinsGTAAC , CM000663.2:g.114705925_114705929delinsGTAAC	GRCh38
NC_000001.10:g.115248546_115248550delinsGTAAC , CM000663.1:g.115248546_115248550delinsGTAAC	GRCh37
NC_000001.9:g.115050069_115050073delinsGTAAC	NCBI36
NG_007572.1:g.15966_15970delinsGTTAC , LRG_92:g.15966_15970delinsGTTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.*2165_*2169delinsGTTAC MANE Select	ENSP00000358548.4:n.*2165_*2169delinsGTTAC
ENST00000369535.4:c.*2165_*2169delinsGTTAC	ENSP00000358548.4:n.*2165_*2169delinsGTTAC
NM_002524.4:c.*2165_*2169delinsGTTAC	NP_002515.1:n.*2165_*2169delinsGTTAC
NM_002524.5:c.*2165_*2169delinsGTTAC MANE Select	NP_002515.1:n.*2165_*2169delinsGTTAC