Canonical Allele Identifier: CA1169548198
Gene: JUN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782679G= , CM000663.2:g.58782679G= GRCh38
NC_000001.10:g.59248351G= , CM000663.1:g.59248351G= GRCh37
NC_000001.9:g.59020939G= NCBI36
NG_047027.1:g.6435C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.458C= ENSP00000518166.1:p.Thr153=
ENST00000371222.4:c.392C= MANE Select ENSP00000360266.2:p.Thr131=
ENST00000678696.1:c.392C= ENSP00000503132.1:p.Thr131=
ENST00000371222.3:c.392C= ENSP00000360266.2:p.Thr131=
NM_002228.3:c.392C= NP_002219.1:p.Thr131=
NM_002228.4:c.392C= MANE Select NP_002219.1:p.Thr131=