Canonical Allele Identifier: CA2333879195

Gene: TYROBP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35908231A= , CM000681.2:g.35908231A=	GRCh38
NC_000019.9:g.36399133A= , CM000681.1:g.36399133A=	GRCh37
NC_000019.8:g.41090973A=	NCBI36
NG_009304.1:g.5054T= , LRG_607:g.5054T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262629.9:c.-3T= MANE Select	ENSP00000262629.3:n.-3T=
ENST00000262629.8:c.-3T=	ENSP00000262629.3:n.-3T=
ENST00000424586.7:c.-3T=	ENSP00000402371.3:n.-3T=
ENST00000544690.6:c.-3T=	ENSP00000445332.1:n.-3T=
ENST00000585626.1:n.65T=
ENST00000585901.6:c.-3T=	ENSP00000468608.1:n.-3T=
ENST00000586946.1:c.-3T=	ENSP00000465656.1:n.-3T=
ENST00000587837.5:c.-3T=	ENSP00000465081.1:n.-3T=
ENST00000589517.1:c.-3T=	ENSP00000468447.1:n.-3T=
NM_001173514.1:c.-3T=	NP_001166985.1:n.-3T=
NM_001173515.1:c.-3T=	NP_001166986.1:n.-3T=
NM_003332.3:c.-3T= , LRG_607t1:c.-3T=	NP_003323.1:n.-3T=
NM_198125.2:c.-3T=	NP_937758.1:n.-3T=
NR_033390.1:n.79T=
NM_001173514.2:c.-3T=	NP_001166985.1:n.-3T=
NM_001173515.2:c.-3T=	NP_001166986.1:n.-3T=
NM_003332.4:c.-3T= MANE Select	NP_003323.1:n.-3T=
NM_198125.3:c.-3T=	NP_937758.1:n.-3T=
NR_033390.2:n.65T=