Canonical Allele Identifier: CA645617028

Gene: TYROBP

Linked Data

• COSMIC: COSM3734793

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35907474del , CM000681.2:g.35907474del	GRCh38
NC_000019.9:g.36398376del , CM000681.1:g.36398376del	GRCh37
NC_000019.8:g.41090216del	NCBI36
NG_009304.1:g.5812del , LRG_607:g.5812del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262629.9:c.202del MANE Select	ENSP00000262629.3:p.Val68SerfsTer?
ENST00000262629.8:c.202del	ENSP00000262629.3:p.Val68SerfsTer?
ENST00000424586.7:c.169del	ENSP00000402371.3:p.Val57SerfsTer?
ENST00000544690.6:c.169del	ENSP00000445332.1:p.Val57SerfsTer?
ENST00000585626.1:n.269del
ENST00000585901.6:c.202del	ENSP00000468608.1:p.Val68SerfsTer12
ENST00000586946.1:c.*87del	ENSP00000465656.1:n.*87del
ENST00000587837.5:c.*87del	ENSP00000465081.1:n.*87del
ENST00000588439.1:n.346del
ENST00000589517.1:c.202del	ENSP00000468447.1:p.Val68SerfsTer?
NM_001173514.1:c.169del	NP_001166985.1:p.Val57SerfsTer?
NM_001173515.1:c.169del	NP_001166986.1:p.Val57SerfsTer?
NM_003332.3:c.202del , LRG_607t1:c.202del	NP_003323.1:p.Val68SerfsTer?
NM_198125.2:c.202del	NP_937758.1:p.Val68SerfsTer?
NR_033390.1:n.243del
NM_001173514.2:c.169del	NP_001166985.1:p.Val57SerfsTer?
NM_001173515.2:c.169del	NP_001166986.1:p.Val57SerfsTer?
NM_003332.4:c.202del MANE Select	NP_003323.1:p.Val68SerfsTer?
NM_198125.3:c.202del	NP_937758.1:p.Val68SerfsTer?
NR_033390.2:n.229del