Canonical Allele Identifier: CA418188713

Gene: JUN

Linked Data

• MyVariant Identifiers: chr1:g.59248398C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.58782726C>T , CM000663.2:g.58782726C>T	GRCh38
NC_000001.10:g.59248398C>T , CM000663.1:g.59248398C>T	GRCh37
NC_000001.9:g.59020986C>T	NCBI36
NG_047027.1:g.6388G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710273.1:c.411G>A	ENSP00000518166.1:p.Val137=
ENST00000371222.4:c.345G>A MANE Select	ENSP00000360266.2:p.Val115=
ENST00000678696.1:c.345G>A	ENSP00000503132.1:p.Val115=
ENST00000371222.3:c.345G>A	ENSP00000360266.2:p.Val115=
NM_002228.3:c.345G>A	NP_002219.1:p.Val115=
NM_002228.4:c.345G>A MANE Select	NP_002219.1:p.Val115=