Canonical Allele Identifier: CA1169548135
Gene: JUN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782557T= , CM000663.2:g.58782557T= GRCh38
NC_000001.10:g.59248229T= , CM000663.1:g.59248229T= GRCh37
NC_000001.9:g.59020817T= NCBI36
NG_047027.1:g.6557A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.580A= ENSP00000518166.1:p.Asn194=
ENST00000371222.4:c.514A= MANE Select ENSP00000360266.2:p.Asn172=
ENST00000678696.1:c.514A= ENSP00000503132.1:p.Asn172=
ENST00000371222.3:c.514A= ENSP00000360266.2:p.Asn172=
NM_002228.3:c.514A= NP_002219.1:p.Asn172=
NM_002228.4:c.514A= MANE Select NP_002219.1:p.Asn172=