Canonical Allele Identifier: CA995498128
Gene: TYROBP HGNC NCBI

Linked Data

dbSNP Id: rs1975755275

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35907467_35907483del , CM000681.2:g.35907467_35907483del GRCh38
NC_000019.9:g.36398369_36398385del , CM000681.1:g.36398369_36398385del GRCh37
NC_000019.8:g.41090209_41090225del NCBI36
NG_009304.1:g.5805_5821del , LRG_607:g.5805_5821del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262629.9:c.195_211del MANE Select ENSP00000262629.3:p.Arg66AlafsTer15
ENST00000262629.8:c.195_211del ENSP00000262629.3:p.Arg66AlafsTer15
ENST00000424586.7:c.162_178del ENSP00000402371.3:p.Arg55AlafsTer14
ENST00000544690.6:c.162_178del ENSP00000445332.1:p.Arg55AlafsTer15
ENST00000585626.1:n.262_278del
ENST00000585901.6:c.195_211del ENSP00000468608.1:p.Arg66AlafsTer16
ENST00000586946.1:c.*80_*96del ENSP00000465656.1:n.*80_*96del
ENST00000587837.5:c.*80_*96del ENSP00000465081.1:n.*80_*96del
ENST00000588439.1:n.339_355del
ENST00000589517.1:c.195_211del ENSP00000468447.1:p.Arg66AlafsTer14
NM_001173514.1:c.162_178del NP_001166985.1:p.Arg55AlafsTer15
NM_001173515.1:c.162_178del NP_001166986.1:p.Arg55AlafsTer14
NM_003332.3:c.195_211del , LRG_607t1:c.195_211del NP_003323.1:p.Arg66AlafsTer15
NM_198125.2:c.195_211del NP_937758.1:p.Arg66AlafsTer14
NR_033390.1:n.236_252del
NM_001173514.2:c.162_178del NP_001166985.1:p.Arg55AlafsTer15
NM_001173515.2:c.162_178del NP_001166986.1:p.Arg55AlafsTer14
NM_003332.4:c.195_211del MANE Select NP_003323.1:p.Arg66AlafsTer15
NM_198125.3:c.195_211del NP_937758.1:p.Arg66AlafsTer14
NR_033390.2:n.222_238del