Canonical Allele Identifier: CA2839133291
Gene: TYROBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35907555del , CM000681.2:g.35907555del GRCh38
NC_000019.9:g.36398457del , CM000681.1:g.36398457del GRCh37
NC_000019.8:g.41090297del NCBI36
NG_009304.1:g.5732del , LRG_607:g.5732del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262629.9:c.122del MANE Select ENSP00000262629.3:p.Gly41AlafsTer7
ENST00000262629.8:c.122del ENSP00000262629.3:p.Gly41AlafsTer7
ENST00000424586.7:c.89del ENSP00000402371.3:p.Gly30AlafsTer7
ENST00000544690.6:c.89del ENSP00000445332.1:p.Gly30AlafsTer7
ENST00000585626.1:n.189del
ENST00000585901.6:c.122del ENSP00000468608.1:p.Gly41AlafsTer7
ENST00000586946.1:c.*7del ENSP00000465656.1:n.*7del
ENST00000587837.5:c.*7del ENSP00000465081.1:n.*7del
ENST00000588439.1:n.266del
ENST00000589517.1:c.122del ENSP00000468447.1:p.Gly41AlafsTer7
NM_001173514.1:c.89del NP_001166985.1:p.Gly30AlafsTer7
NM_001173515.1:c.89del NP_001166986.1:p.Gly30AlafsTer7
NM_003332.3:c.122del , LRG_607t1:c.122del NP_003323.1:p.Gly41AlafsTer7
NM_198125.2:c.122del NP_937758.1:p.Gly41AlafsTer7
NR_033390.1:n.163del
NM_001173514.2:c.89del NP_001166985.1:p.Gly30AlafsTer7
NM_001173515.2:c.89del NP_001166986.1:p.Gly30AlafsTer7
NM_003332.4:c.122del MANE Select NP_003323.1:p.Gly41AlafsTer7
NM_198125.3:c.122del NP_937758.1:p.Gly41AlafsTer7
NR_033390.2:n.149del