Canonical Allele Identifier: CA340577442

Gene: JUN

Linked Data

• gnomAD v4: 1-58782226-T-A
• MyVariant Identifiers: chr1:g.59247898T>A (hg19) ; chr1:g.58782226T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.58782226T>A , CM000663.2:g.58782226T>A	GRCh38
NC_000001.10:g.59247898T>A , CM000663.1:g.59247898T>A	GRCh37
NC_000001.9:g.59020486T>A	NCBI36
NG_047027.1:g.6888A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000710273.1:c.911A>T	ENSP00000518166.1:p.Glu304Val
ENST00000371222.4:c.845A>T MANE Select	ENSP00000360266.2:p.Glu282Val
ENST00000678696.1:c.845A>T	ENSP00000503132.1:p.Glu282Val
ENST00000371222.3:c.845A>T	ENSP00000360266.2:p.Glu282Val
NM_002228.3:c.845A>T	NP_002219.1:p.Glu282Val
NM_002228.4:c.845A>T MANE Select	NP_002219.1:p.Glu282Val