Canonical Allele Identifier: CA1190291306

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713908_114713909delinsTG , CM000663.2:g.114713908_114713909delinsTG	GRCh38
NC_000001.10:g.115256529_115256530delinsTG , CM000663.1:g.115256529_115256530delinsTG	GRCh37
NC_000001.9:g.115058052_115058053delinsTG	NCBI36
NG_007572.1:g.7986_7987delinsCA , LRG_92:g.7986_7987delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000369535.5:c.181_182delinsCA MANE Select	ENSP00000358548.4:p.Gln61=
ENST00000369535.4:c.181_182delinsCA	ENSP00000358548.4:p.Gln61=
NM_002524.4:c.181_182delinsCA	NP_002515.1:p.Gln61=
NM_002524.5:c.181_182delinsCA MANE Select	NP_002515.1:p.Gln61=