Canonical Allele Identifier: CA525409585
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1272661723
gnomAD v2: 1-115256812-C-CTA
gnomAD v3: 1-114714191-C-CTA
gnomAD v4: 1-114714191-C-CTA
MyVariant Identifiers: chr1:g.115256812_115256813insTA (hg19) chr1:g.114714191_114714192insTA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114714195_114714196dup , CM000663.2:g.114714195_114714196dup GRCh38
NC_000001.10:g.115256816_115256817dup , CM000663.1:g.115256816_115256817dup GRCh37
NC_000001.9:g.115058339_115058340dup NCBI36
NG_007572.1:g.7702_7703dup , LRG_92:g.7702_7703dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.112-215_112-214dup MANE Select ENSP00000358548.4:n.112-215_112-214dup
ENST00000369535.4:c.112-215_112-214dup ENSP00000358548.4:n.112-215_112-214dup
NM_002524.4:c.112-215_112-214dup NP_002515.1:n.112-215_112-214dup
NM_002524.5:c.112-215_112-214dup MANE Select NP_002515.1:n.112-215_112-214dup
Search 100 bp 5'
Search 100 bp 3'