Canonical Allele Identifier: CA2745134311

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114705243dup , CM000663.2:g.114705243dup	GRCh38
NC_000001.10:g.115247864dup , CM000663.1:g.115247864dup	GRCh37
NC_000001.9:g.115049387dup	NCBI36
NG_007572.1:g.16652dup , LRG_92:g.16652dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000369535.5:c.*2851dup MANE Select	ENSP00000358548.4:n.*2851dup
ENST00000369535.4:c.*2851dup	ENSP00000358548.4:n.*2851dup
NM_002524.4:c.*2851dup	NP_002515.1:n.*2851dup
NM_002524.5:c.*2851dup MANE Select	NP_002515.1:n.*2851dup