Canonical Allele Identifier: CA885828049
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs869069547
gnomAD v4: 1-114709465-GA-G
MyVariant Identifiers: chr1:g.115252087del (hg19) chr1:g.114709466del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709472del , CM000663.2:g.114709472del GRCh38
NC_000001.10:g.115252093del , CM000663.1:g.115252093del GRCh37
NC_000001.9:g.115053616del NCBI36
NG_007572.1:g.12429del , LRG_92:g.12429del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.450+103del MANE Select ENSP00000358548.4:n.450+103del
ENST00000369535.4:c.450+103del ENSP00000358548.4:n.450+103del
NM_002524.4:c.450+103del NP_002515.1:n.450+103del
NM_002524.5:c.450+103del MANE Select NP_002515.1:n.450+103del
Search 100 bp 5'
Search 100 bp 3'