Canonical Allele Identifier: CA2647251646
Gene: NRAS HGNC NCBI

Linked Data

gnomAD v4: 1-114708105-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114708105A>T , CM000663.2:g.114708105A>T GRCh38
NC_000001.10:g.115250726A>T , CM000663.1:g.115250726A>T GRCh37
NC_000001.9:g.115052249A>T NCBI36
NG_007572.1:g.13790T>A , LRG_92:g.13790T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*43+49T>A MANE Select ENSP00000358548.4:n.*43+49T>A
ENST00000369535.4:c.*43+49T>A ENSP00000358548.4:n.*43+49T>A
NM_002524.4:c.*43+49T>A NP_002515.1:n.*43+49T>A
NM_002524.5:c.*43+49T>A MANE Select NP_002515.1:n.*43+49T>A
Search 100 bp 5'
Search 100 bp 3'