Canonical Allele Identifier: CA1020728

Gene: NRAS

Linked Data

• ClinVar Variation Id: 764200
• ClinVar RCV Id: RCV001456038
• dbSNP Id: rs575693594
• ExAC: 1:115252340 A / T
• gnomAD v2: 1-115252340-A-T
• gnomAD v3: 1-114709719-A-T
• gnomAD v4: 1-114709719-A-T
• MyVariant Identifiers: chr1:g.115252340A>T (hg19) ; chr1:g.114709719A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709719A>T , CM000663.2:g.114709719A>T	GRCh38
NC_000001.10:g.115252340A>T , CM000663.1:g.115252340A>T	GRCh37
NC_000001.9:g.115053863A>T	NCBI36
NG_007572.1:g.12176T>A , LRG_92:g.12176T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.300T>A MANE Select	ENSP00000358548.4:p.Ile100=
ENST00000369535.4:c.300T>A	ENSP00000358548.4:p.Ile100=
NM_002524.4:c.300T>A	NP_002515.1:p.Ile100=
NM_002524.5:c.300T>A MANE Select	NP_002515.1:p.Ile100=