Canonical Allele Identifier: CA1144330701
Gene: JUN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782477G= , CM000663.2:g.58782477G= GRCh38
NC_000001.10:g.59248149G= , CM000663.1:g.59248149G= GRCh37
NC_000001.9:g.59020737G= NCBI36
NG_047027.1:g.6637C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.660C= ENSP00000518166.1:p.Pro220=
ENST00000371222.4:c.594C= MANE Select ENSP00000360266.2:p.Pro198=
ENST00000678696.1:c.594C= ENSP00000503132.1:p.Pro198=
ENST00000371222.3:c.594C= ENSP00000360266.2:p.Pro198=
NM_002228.3:c.594C= NP_002219.1:p.Pro198=
NM_002228.4:c.594C= MANE Select NP_002219.1:p.Pro198=