Canonical Allele Identifier: CA2645908855
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs1553147012

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782738_58782749del , CM000663.2:g.58782738_58782749del GRCh38
NC_000001.10:g.59248410_59248421del , CM000663.1:g.59248410_59248421del GRCh37
NC_000001.9:g.59020998_59021009del NCBI36
NG_047027.1:g.6375_6386del

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.398_409del ENSP00000518166.1:p.Ala133_Phe136del
ENST00000371222.4:c.332_343del MANE Select ENSP00000360266.2:p.Ala111_Phe114del
ENST00000678696.1:c.332_343del ENSP00000503132.1:p.Ala111_Phe114del
ENST00000371222.3:c.332_343del ENSP00000360266.2:p.Ala111_Phe114del
NM_002228.3:c.332_343del NP_002219.1:p.Ala111_Phe114del
NM_002228.4:c.332_343del MANE Select NP_002219.1:p.Ala111_Phe114del