Canonical Allele Identifier: CA885830216
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1426563777
gnomAD v3: 1-114713794-T-TA
gnomAD v4: 1-114713794-T-TA
MyVariant Identifiers: chr1:g.115256415_115256416insA (hg19) chr1:g.114713794_114713795insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713795dup , CM000663.2:g.114713795dup GRCh38
NC_000001.10:g.115256416dup , CM000663.1:g.115256416dup GRCh37
NC_000001.9:g.115057939dup NCBI36
NG_007572.1:g.8100dup , LRG_92:g.8100dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.290+5dup MANE Select ENSP00000358548.4:n.290+5dup
ENST00000369535.4:c.290+5dup ENSP00000358548.4:n.290+5dup
NM_002524.4:c.290+5dup NP_002515.1:n.290+5dup
NM_002524.5:c.290+5dup MANE Select NP_002515.1:n.290+5dup
Search 100 bp 5'
Search 100 bp 3'