Canonical Allele Identifier: CA1144913553
Gene: JUN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782653C= , CM000663.2:g.58782653C= GRCh38
NC_000001.10:g.59248325C= , CM000663.1:g.59248325C= GRCh37
NC_000001.9:g.59020913C= NCBI36
NG_047027.1:g.6461G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.484G= ENSP00000518166.1:p.Ala162=
ENST00000371222.4:c.418G= MANE Select ENSP00000360266.2:p.Ala140=
ENST00000678696.1:c.418G= ENSP00000503132.1:p.Ala140=
ENST00000371222.3:c.418G= ENSP00000360266.2:p.Ala140=
NM_002228.3:c.418G= NP_002219.1:p.Ala140=
NM_002228.4:c.418G= MANE Select NP_002219.1:p.Ala140=