Canonical Allele Identifier: CA16602362

Gene: NRAS

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713909G>C , CM000663.2:g.114713909G>C	GRCh38
NC_000001.10:g.115256530G>C , CM000663.1:g.115256530G>C	GRCh37
NC_000001.9:g.115058053G>C	NCBI36
NG_007572.1:g.7986C>G , LRG_92:g.7986C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.181C>G MANE Select	ENSP00000358548.4:p.Gln61Glu
ENST00000369535.4:c.181C>G	ENSP00000358548.4:p.Gln61Glu
NM_002524.4:c.181C>G	NP_002515.1:p.Gln61Glu
NM_002524.5:c.181C>G MANE Select	NP_002515.1:p.Gln61Glu