Canonical Allele Identifier: CA1169548115
Gene: JUN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782515_58782548delinsCGCCGCCGCTGCTCAGCGCGCCTGGGTTGAAGTT , CM000663.2:g.58782515_58782548delinsCGCCGCCGCTGCTCAGCGCGCCTGGGTTGAAGTT GRCh38
NC_000001.10:g.59248187_59248220delinsCGCCGCCGCTGCTCAGCGCGCCTGGGTTGAAGTT , CM000663.1:g.59248187_59248220delinsCGCCGCCGCTGCTCAGCGCGCCTGGGTTGAAGTT GRCh37
NC_000001.9:g.59020775_59020808delinsCGCCGCCGCTGCTCAGCGCGCCTGGGTTGAAGTT NCBI36
NG_047027.1:g.6566_6599delinsAACTTCAACCCAGGCGCGCTGAGCAGCGGCGGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.589_622delinsAACTTCAACCCAGGCGCGCTGAGCAGCGGCGGCG ENSP00000518166.1:p.Asn197=
ENST00000371222.4:c.523_556delinsAACTTCAACCCAGGCGCGCTGAGCAGCGGCGGCG MANE Select ENSP00000360266.2:p.Asn175=
ENST00000678696.1:c.523_556delinsAACTTCAACCCAGGCGCGCTGAGCAGCGGCGGCG ENSP00000503132.1:p.Asn175=
ENST00000371222.3:c.523_556delinsAACTTCAACCCAGGCGCGCTGAGCAGCGGCGGCG ENSP00000360266.2:p.Asn175=
NM_002228.3:c.523_556delinsAACTTCAACCCAGGCGCGCTGAGCAGCGGCGGCG NP_002219.1:p.Asn175=
NM_002228.4:c.523_556delinsAACTTCAACCCAGGCGCGCTGAGCAGCGGCGGCG MANE Select NP_002219.1:p.Asn175=