Canonical Allele Identifier: CA1020761
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 561348
ClinVar RCV Id: RCV000680633 RCV001193081 RCV002060861
dbSNP Id: rs780595451
ExAC: 1:115256618 A / AG
gnomAD v2: 1-115256618-A-AG
gnomAD v3: 1-114713997-A-AG
gnomAD v4: 1-114713997-A-AG
MyVariant Identifiers: chr1:g.115256619dup (hg19) chr1:g.115256618_115256619insG (hg19) chr1:g.114713998dup (hg38) chr1:g.114713997_114713998insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114714002dup , CM000663.2:g.114714002dup GRCh38
NC_000001.10:g.115256623dup , CM000663.1:g.115256623dup GRCh37
NC_000001.9:g.115058146dup NCBI36
NG_007572.1:g.7897dup , LRG_92:g.7897dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.112-20dup MANE Select ENSP00000358548.4:n.112-20dup
ENST00000369535.4:c.112-20dup ENSP00000358548.4:n.112-20dup
NM_002524.4:c.112-20dup NP_002515.1:n.112-20dup
NM_002524.5:c.112-20dup MANE Select NP_002515.1:n.112-20dup
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Search 100 bp 3'