Canonical Allele Identifier: CA2540186552
Gene: NRAS HGNC NCBI

Linked Data

gnomAD v4: 1-114709433-T-TAA
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709441_114709442dup , CM000663.2:g.114709441_114709442dup GRCh38
NC_000001.10:g.115252062_115252063dup , CM000663.1:g.115252062_115252063dup GRCh37
NC_000001.9:g.115053585_115053586dup NCBI36
NG_007572.1:g.12460_12461dup , LRG_92:g.12460_12461dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.450+134_450+135dup MANE Select ENSP00000358548.4:n.450+134_450+135dup
ENST00000369535.4:c.450+134_450+135dup ENSP00000358548.4:n.450+134_450+135dup
NM_002524.4:c.450+134_450+135dup NP_002515.1:n.450+134_450+135dup
NM_002524.5:c.450+134_450+135dup MANE Select NP_002515.1:n.450+134_450+135dup
Search 100 bp 5'
Search 100 bp 3'