Canonical Allele Identifier: CA2647248224

Gene: NRAS

Linked Data

• gnomAD v4: 1-114713684-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713684A>G , CM000663.2:g.114713684A>G	GRCh38
NC_000001.10:g.115256305A>G , CM000663.1:g.115256305A>G	GRCh37
NC_000001.9:g.115057828A>G	NCBI36
NG_007572.1:g.8211T>C , LRG_92:g.8211T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.290+116T>C MANE Select	ENSP00000358548.4:n.290+116T>C
ENST00000369535.4:c.290+116T>C	ENSP00000358548.4:n.290+116T>C
NM_002524.4:c.290+116T>C	NP_002515.1:n.290+116T>C
NM_002524.5:c.290+116T>C MANE Select	NP_002515.1:n.290+116T>C