Canonical Allele Identifier: CA1169548097
Gene: JUN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782482A= , CM000663.2:g.58782482A= GRCh38
NC_000001.10:g.59248154A= , CM000663.1:g.59248154A= GRCh37
NC_000001.9:g.59020742A= NCBI36
NG_047027.1:g.6632T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.655T= ENSP00000518166.1:p.Phe219=
ENST00000371222.4:c.589T= MANE Select ENSP00000360266.2:p.Phe197=
ENST00000678696.1:c.589T= ENSP00000503132.1:p.Phe197=
ENST00000371222.3:c.589T= ENSP00000360266.2:p.Phe197=
NM_002228.3:c.589T= NP_002219.1:p.Phe197=
NM_002228.4:c.589T= MANE Select NP_002219.1:p.Phe197=