Canonical Allele Identifier: CA418189076

Gene: JUN

Linked Data

• MyVariant Identifiers: chr1:g.59248353G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.58782681G>T , CM000663.2:g.58782681G>T	GRCh38
NC_000001.10:g.59248353G>T , CM000663.1:g.59248353G>T	GRCh37
NC_000001.9:g.59020941G>T	NCBI36
NG_047027.1:g.6433C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710273.1:c.456C>A	ENSP00000518166.1:p.Val152=
ENST00000371222.4:c.390C>A MANE Select	ENSP00000360266.2:p.Val130=
ENST00000678696.1:c.390C>A	ENSP00000503132.1:p.Val130=
ENST00000371222.3:c.390C>A	ENSP00000360266.2:p.Val130=
NM_002228.3:c.390C>A	NP_002219.1:p.Val130=
NM_002228.4:c.390C>A MANE Select	NP_002219.1:p.Val130=