Canonical Allele Identifier: CA2584619516

Gene: TYROBP

Linked Data

• gnomAD v4: 19-35907552-G-GC

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262629.9:c.122dup MANE Select	ENSP00000262629.3:p.Val42ArgfsTer?
ENST00000262629.8:c.122dup	ENSP00000262629.3:p.Val42ArgfsTer?
ENST00000424586.7:c.89dup	ENSP00000402371.3:p.Val31ArgfsTer?
ENST00000544690.6:c.89dup	ENSP00000445332.1:p.Val31ArgfsTer?
ENST00000585626.1:n.189dup
ENST00000585901.6:c.122dup	ENSP00000468608.1:p.Val42ArgfsTer?
ENST00000586946.1:c.*7dup	ENSP00000465656.1:n.*7dup
ENST00000587837.5:c.*7dup	ENSP00000465081.1:n.*7dup
ENST00000588439.1:n.266dup
ENST00000589517.1:c.122dup	ENSP00000468447.1:p.Val42ArgfsTer?
NM_001173514.1:c.89dup	NP_001166985.1:p.Val31ArgfsTer?
NM_001173515.1:c.89dup	NP_001166986.1:p.Val31ArgfsTer?
NM_003332.3:c.122dup , LRG_607t1:c.122dup	NP_003323.1:p.Val42ArgfsTer?
NM_198125.2:c.122dup	NP_937758.1:p.Val42ArgfsTer?
NR_033390.1:n.163dup
NM_001173514.2:c.89dup	NP_001166985.1:p.Val31ArgfsTer?
NM_001173515.2:c.89dup	NP_001166986.1:p.Val31ArgfsTer?
NM_003332.4:c.122dup MANE Select	NP_003323.1:p.Val42ArgfsTer?
NM_198125.3:c.122dup	NP_937758.1:p.Val42ArgfsTer?
NR_033390.2:n.149dup