Canonical Allele Identifier: CA1148724608
Gene: JUN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782645C= , CM000663.2:g.58782645C= GRCh38
NC_000001.10:g.59248317C= , CM000663.1:g.59248317C= GRCh37
NC_000001.9:g.59020905C= NCBI36
NG_047027.1:g.6469G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.492G= ENSP00000518166.1:p.Met164=
ENST00000371222.4:c.426G= MANE Select ENSP00000360266.2:p.Met142=
ENST00000678696.1:c.426G= ENSP00000503132.1:p.Met142=
ENST00000371222.3:c.426G= ENSP00000360266.2:p.Met142=
NM_002228.3:c.426G= NP_002219.1:p.Met142=
NM_002228.4:c.426G= MANE Select NP_002219.1:p.Met142=