Canonical Allele Identifier: CA1190291411

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114714201_114714202delinsGC , CM000663.2:g.114714201_114714202delinsGC	GRCh38
NC_000001.10:g.115256822_115256823delinsGC , CM000663.1:g.115256822_115256823delinsGC	GRCh37
NC_000001.9:g.115058345_115058346delinsGC	NCBI36
NG_007572.1:g.7693_7694delinsGC , LRG_92:g.7693_7694delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.112-224_112-223delinsGC MANE Select	ENSP00000358548.4:n.112-224_112-223delinsGC
ENST00000369535.4:c.112-224_112-223delinsGC	ENSP00000358548.4:n.112-224_112-223delinsGC
NM_002524.4:c.112-224_112-223delinsGC	NP_002515.1:n.112-224_112-223delinsGC
NM_002524.5:c.112-224_112-223delinsGC MANE Select	NP_002515.1:n.112-224_112-223delinsGC