Canonical Allele Identifier: CA878286
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs748534142
ExAC: 1:59248123 G / GGCTGCT
gnomAD v2: 1-59248123-G-GGCTGCT
gnomAD v3: 1-58782451-G-GGCTGCT
gnomAD v4: 1-58782451-G-GGCTGCT
MyVariant Identifiers: chr1:g.59248129_59248130insGCTGCT (hg19) chr1:g.59248123_59248124insGCTGCT (hg19) chr1:g.58782457_58782458insGCTGCT (hg38) chr1:g.58782451_58782452insGCTGCT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782462_58782467dup , CM000663.2:g.58782462_58782467dup GRCh38
NC_000001.10:g.59248134_59248139dup , CM000663.1:g.59248134_59248139dup GRCh37
NC_000001.9:g.59020722_59020727dup NCBI36
NG_047027.1:g.6657_6662dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.680_685dup ENSP00000518166.1:p.Gln228_Pro229insGlnGln
ENST00000371222.4:c.614_619dup MANE Select ENSP00000360266.2:p.Gln206_Pro207insGlnGln
ENST00000678696.1:c.614_619dup ENSP00000503132.1:p.Gln206_Pro207insGlnGln
ENST00000371222.3:c.614_619dup ENSP00000360266.2:p.Gln206_Pro207insGlnGln
NM_002228.3:c.614_619dup NP_002219.1:p.Gln206_Pro207insGlnGln
NM_002228.4:c.614_619dup MANE Select NP_002219.1:p.Gln206_Pro207insGlnGln
Search 100 bp 5'
Search 100 bp 3'