Canonical Allele Identifier: CA525409522
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1274191530
gnomAD v2: 1-115256096-TTACA-T
gnomAD v3: 1-114713475-TTACA-T
gnomAD v4: 1-114713475-TTACA-T
MyVariant Identifiers: chr1:g.115256097_115256100del (hg19) chr1:g.114713476_114713479del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713479_114713482del , CM000663.2:g.114713479_114713482del GRCh38
NC_000001.10:g.115256100_115256103del , CM000663.1:g.115256100_115256103del GRCh37
NC_000001.9:g.115057623_115057626del NCBI36
NG_007572.1:g.8416_8419del , LRG_92:g.8416_8419del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.290+321_290+324del MANE Select ENSP00000358548.4:n.290+321_290+324del
ENST00000369535.4:c.290+321_290+324del ENSP00000358548.4:n.290+321_290+324del
NM_002524.4:c.290+321_290+324del NP_002515.1:n.290+321_290+324del
NM_002524.5:c.290+321_290+324del MANE Select NP_002515.1:n.290+321_290+324del
Search 100 bp 5'
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