Canonical Allele Identifier: CA418188729

Gene: JUN

Linked Data

• MyVariant Identifiers: chr1:g.59248149G>T (hg19)

Genomic Alleles

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

Transcript Alleles

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