Canonical Allele Identifier: CA1169548129
Gene: JUN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782541T= , CM000663.2:g.58782541T= GRCh38
NC_000001.10:g.59248213T= , CM000663.1:g.59248213T= GRCh37
NC_000001.9:g.59020801T= NCBI36
NG_047027.1:g.6573A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.596A= ENSP00000518166.1:p.Asn199=
ENST00000371222.4:c.530A= MANE Select ENSP00000360266.2:p.Asn177=
ENST00000678696.1:c.530A= ENSP00000503132.1:p.Asn177=
ENST00000371222.3:c.530A= ENSP00000360266.2:p.Asn177=
NM_002228.3:c.530A= NP_002219.1:p.Asn177=
NM_002228.4:c.530A= MANE Select NP_002219.1:p.Asn177=