Canonical Allele Identifier: CA2647250082

Gene: NRAS

Linked Data

• gnomAD v4: 1-114705694-A-ACTG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114705695_114705697dup , CM000663.2:g.114705695_114705697dup	GRCh38
NC_000001.10:g.115248316_115248318dup , CM000663.1:g.115248316_115248318dup	GRCh37
NC_000001.9:g.115049839_115049841dup	NCBI36
NG_007572.1:g.16198_16200dup , LRG_92:g.16198_16200dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.*2397_*2399dup MANE Select	ENSP00000358548.4:n.*2397_*2399dup
ENST00000369535.4:c.*2397_*2399dup	ENSP00000358548.4:n.*2397_*2399dup
NM_002524.4:c.*2397_*2399dup	NP_002515.1:n.*2397_*2399dup
NM_002524.5:c.*2397_*2399dup MANE Select	NP_002515.1:n.*2397_*2399dup