Canonical Allele Identifier: CA10607584

Gene: NRAS

Linked Data

• ClinVar Variation Id: 291949
• ClinVar RCV Id: RCV000304039 ; RCV003409429
• dbSNP Id: rs776606789
• gnomAD v2: 1-115247910-A-G
• gnomAD v3: 1-114705289-A-G
• gnomAD v4: 1-114705289-A-G
• MyVariant Identifiers: chr1:g.115247910A>G (hg19) ; chr1:g.114705289A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114705289A>G , CM000663.2:g.114705289A>G	GRCh38
NC_000001.10:g.115247910A>G , CM000663.1:g.115247910A>G	GRCh37
NC_000001.9:g.115049433A>G	NCBI36
NG_007572.1:g.16606T>C , LRG_92:g.16606T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.*2805T>C MANE Select	ENSP00000358548.4:n.*2805T>C
ENST00000369535.4:c.*2805T>C	ENSP00000358548.4:n.*2805T>C
NM_002524.4:c.*2805T>C	NP_002515.1:n.*2805T>C
NM_002524.5:c.*2805T>C MANE Select	NP_002515.1:n.*2805T>C