Canonical Allele Identifier: CA340578442
Gene: JUN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782695T>G , CM000663.2:g.58782695T>G GRCh38
NC_000001.10:g.59248367T>G , CM000663.1:g.59248367T>G GRCh37
NC_000001.9:g.59020955T>G NCBI36
NG_047027.1:g.6419A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.442A>C ENSP00000518166.1:p.Thr148Pro
ENST00000371222.4:c.376A>C MANE Select ENSP00000360266.2:p.Thr126Pro
ENST00000678696.1:c.376A>C ENSP00000503132.1:p.Thr126Pro
ENST00000371222.3:c.376A>C ENSP00000360266.2:p.Thr126Pro
NM_002228.3:c.376A>C NP_002219.1:p.Thr126Pro
NM_002228.4:c.376A>C MANE Select NP_002219.1:p.Thr126Pro