Canonical Allele Identifier: CA1190289436

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709477_114709480delinsTAAC , CM000663.2:g.114709477_114709480delinsTAAC	GRCh38
NC_000001.10:g.115252098_115252101delinsTAAC , CM000663.1:g.115252098_115252101delinsTAAC	GRCh37
NC_000001.9:g.115053621_115053624delinsTAAC	NCBI36
NG_007572.1:g.12415_12418delinsGTTA , LRG_92:g.12415_12418delinsGTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.450+89_450+92delinsGTTA MANE Select	ENSP00000358548.4:n.450+89_450+92delinsGTTA
ENST00000369535.4:c.450+89_450+92delinsGTTA	ENSP00000358548.4:n.450+89_450+92delinsGTTA
NM_002524.4:c.450+89_450+92delinsGTTA	NP_002515.1:n.450+89_450+92delinsGTTA
NM_002524.5:c.450+89_450+92delinsGTTA MANE Select	NP_002515.1:n.450+89_450+92delinsGTTA