Canonical Allele Identifier: CA9393104

Gene: TYROBP

Linked Data

• dbSNP Id: rs751794674
• ExAC: 19:36398467 G / GT
• MyVariant Identifiers: chr19:g.36398467_36398468insT (hg19) ; chr19:g.35907565_35907566insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35907566dup , CM000681.2:g.35907566dup	GRCh38
NC_000019.9:g.36398468dup , CM000681.1:g.36398468dup	GRCh37
NC_000019.8:g.41090308dup	NCBI36
NG_009304.1:g.5719dup , LRG_607:g.5719dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262629.9:c.109dup MANE Select	ENSP00000262629.3:p.Thr37AsnfsTer?
ENST00000262629.8:c.109dup	ENSP00000262629.3:p.Thr37AsnfsTer?
ENST00000424586.7:c.76dup	ENSP00000402371.3:p.Thr26AsnfsTer?
ENST00000544690.6:c.76dup	ENSP00000445332.1:p.Thr26AsnfsTer?
ENST00000585626.1:n.176dup
ENST00000585901.6:c.109dup	ENSP00000468608.1:p.Thr37AsnfsTer?
ENST00000586946.1:c.102dup	ENSP00000465656.1:p.Arg35ThrfsTer?
ENST00000587837.5:c.102dup	ENSP00000465081.1:p.Arg35ThrfsTer?
ENST00000588439.1:n.253dup
ENST00000589517.1:c.109dup	ENSP00000468447.1:p.Thr37AsnfsTer?
NM_001173514.1:c.76dup	NP_001166985.1:p.Thr26AsnfsTer?
NM_001173515.1:c.76dup	NP_001166986.1:p.Thr26AsnfsTer?
NM_003332.3:c.109dup , LRG_607t1:c.109dup	NP_003323.1:p.Thr37AsnfsTer?
NM_198125.2:c.109dup	NP_937758.1:p.Thr37AsnfsTer?
NR_033390.1:n.150dup
NM_001173514.2:c.76dup	NP_001166985.1:p.Thr26AsnfsTer?
NM_001173515.2:c.76dup	NP_001166986.1:p.Thr26AsnfsTer?
NM_003332.4:c.109dup MANE Select	NP_003323.1:p.Thr37AsnfsTer?
NM_198125.3:c.109dup	NP_937758.1:p.Thr37AsnfsTer?
NR_033390.2:n.136dup