Canonical Allele Identifier: CA1020760
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2728972
ClinVar RCV Id: RCV003540099
dbSNP Id: rs758918340
ExAC: 1:115256616 TA / T
gnomAD v2: 1-115256616-TA-T
gnomAD v3: 1-114713995-TA-T
gnomAD v4: 1-114713995-TA-T
MyVariant Identifiers: chr1:g.115256617del (hg19) chr1:g.114713996del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713997del , CM000663.2:g.114713997del GRCh38
NC_000001.10:g.115256618del , CM000663.1:g.115256618del GRCh37
NC_000001.9:g.115058141del NCBI36
NG_007572.1:g.7899del , LRG_92:g.7899del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.112-18del MANE Select ENSP00000358548.4:n.112-18del
ENST00000369535.4:c.112-18del ENSP00000358548.4:n.112-18del
NM_002524.4:c.112-18del NP_002515.1:n.112-18del
NM_002524.5:c.112-18del MANE Select NP_002515.1:n.112-18del
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