Canonical Allele Identifier: CA2333878831

Gene: TYROBP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35907467G= , CM000681.2:g.35907467G=	GRCh38
NC_000019.9:g.36398369G= , CM000681.1:g.36398369G=	GRCh37
NC_000019.8:g.41090209G=	NCBI36
NG_009304.1:g.5818C= , LRG_607:g.5818C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262629.9:c.208C= MANE Select	ENSP00000262629.3:p.Arg70=
ENST00000262629.8:c.208C=	ENSP00000262629.3:p.Arg70=
ENST00000424586.7:c.175C=	ENSP00000402371.3:p.Arg59=
ENST00000544690.6:c.175C=	ENSP00000445332.1:p.Arg59=
ENST00000585626.1:n.275C=
ENST00000585901.6:c.208C=	ENSP00000468608.1:p.Arg70=
ENST00000586946.1:c.*93C=	ENSP00000465656.1:n.*93C=
ENST00000587837.5:c.*93C=	ENSP00000465081.1:n.*93C=
ENST00000588439.1:n.352C=
ENST00000589517.1:c.208C=	ENSP00000468447.1:p.Arg70=
NM_001173514.1:c.175C=	NP_001166985.1:p.Arg59=
NM_001173515.1:c.175C=	NP_001166986.1:p.Arg59=
NM_003332.3:c.208C= , LRG_607t1:c.208C=	NP_003323.1:p.Arg70=
NM_198125.2:c.208C=	NP_937758.1:p.Arg70=
NR_033390.1:n.249C=
NM_001173514.2:c.175C=	NP_001166985.1:p.Arg59=
NM_001173515.2:c.175C=	NP_001166986.1:p.Arg59=
NM_003332.4:c.208C= MANE Select	NP_003323.1:p.Arg70=
NM_198125.3:c.208C=	NP_937758.1:p.Arg70=
NR_033390.2:n.235C=