Canonical Allele Identifier: CA1020709

Gene: NRAS

Linked Data

• ClinVar Variation Id: 515883
• ClinVar RCV Id: RCV000603088 ; RCV002064335 ; RCV001813525 ; RCV002331082
• dbSNP Id: rs753079400
• ExAC: 1:115252208 G / A
• gnomAD v2: 1-115252208-G-A
• gnomAD v3: 1-114709587-G-A
• gnomAD v4: 1-114709587-G-A
• MyVariant Identifiers: chr1:g.115252208G>A (hg19) ; chr1:g.114709587G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709587G>A , CM000663.2:g.114709587G>A	GRCh38
NC_000001.10:g.115252208G>A , CM000663.1:g.115252208G>A	GRCh37
NC_000001.9:g.115053731G>A	NCBI36
NG_007572.1:g.12308C>T , LRG_92:g.12308C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.432C>T MANE Select	ENSP00000358548.4:p.Thr144=
ENST00000369535.4:c.432C>T	ENSP00000358548.4:p.Thr144=
NM_002524.4:c.432C>T	NP_002515.1:p.Thr144=
NM_002524.5:c.432C>T MANE Select	NP_002515.1:p.Thr144=