Canonical Allele Identifier: CA134568

Gene: NRAS

Linked Data

• ClinVar Variation Id: 44575
• ClinVar RCV Id: RCV000037575 ; RCV000862599 ; RCV001707515
• dbSNP Id: rs376187980
• ExAC: 1:115252357 C / T
• gnomAD v2: 1-115252357-C-T
• gnomAD v3: 1-114709736-C-T
• gnomAD v4: 1-114709736-C-T
• MyVariant Identifiers: chr1:g.115252357C>T (hg19) ; chr1:g.114709736C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709736C>T , CM000663.2:g.114709736C>T	GRCh38
NC_000001.10:g.115252357C>T , CM000663.1:g.115252357C>T	GRCh37
NC_000001.9:g.115053880C>T	NCBI36
NG_007572.1:g.12159G>A , LRG_92:g.12159G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.291-8G>A MANE Select	ENSP00000358548.4:n.291-8G>A
ENST00000369535.4:c.291-8G>A	ENSP00000358548.4:n.291-8G>A
NM_002524.4:c.291-8G>A	NP_002515.1:n.291-8G>A
NM_002524.5:c.291-8G>A MANE Select	NP_002515.1:n.291-8G>A