Canonical Allele Identifier: CA878279
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs755197297
ExAC: 1:59248117 T / TGCG
gnomAD v2: 1-59248117-T-TGCG
gnomAD v4: 1-58782445-T-TGCG
MyVariant Identifiers: chr1:g.59248120_59248121insGCG (hg19) chr1:g.59248117_59248118insGCG (hg19) chr1:g.58782448_58782449insGCG (hg38) chr1:g.58782445_58782446insGCG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782451_58782453dup , CM000663.2:g.58782451_58782453dup GRCh38
NC_000001.10:g.59248123_59248125dup , CM000663.1:g.59248123_59248125dup GRCh37
NC_000001.9:g.59020711_59020713dup NCBI36
NG_047027.1:g.6666_6668dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.689_691dup ENSP00000518166.1:p.Pro230_His231insPro
ENST00000371222.4:c.623_625dup MANE Select ENSP00000360266.2:p.Pro208_His209insPro
ENST00000678696.1:c.623_625dup ENSP00000503132.1:p.Pro208_His209insPro
ENST00000371222.3:c.623_625dup ENSP00000360266.2:p.Pro208_His209insPro
NM_002228.3:c.623_625dup NP_002219.1:p.Pro208_His209insPro
NM_002228.4:c.623_625dup MANE Select NP_002219.1:p.Pro208_His209insPro
Search 100 bp 5'
Search 100 bp 3'