Canonical Allele Identifier: CA2333878850

Gene: TYROBP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35907523_35907524delinsAG , CM000681.2:g.35907523_35907524delinsAG	GRCh38
NC_000019.9:g.36398425_36398426delinsAG , CM000681.1:g.36398425_36398426delinsAG	GRCh37
NC_000019.8:g.41090265_41090266delinsAG	NCBI36
NG_009304.1:g.5761_5762delinsCT , LRG_607:g.5761_5762delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262629.9:c.151_152delinsCT MANE Select	ENSP00000262629.3:p.Leu51=
ENST00000262629.8:c.151_152delinsCT	ENSP00000262629.3:p.Leu51=
ENST00000424586.7:c.118_119delinsCT	ENSP00000402371.3:p.Leu40=
ENST00000544690.6:c.118_119delinsCT	ENSP00000445332.1:p.Leu40=
ENST00000585626.1:n.218_219delinsCT
ENST00000585901.6:c.151_152delinsCT	ENSP00000468608.1:p.Leu51=
ENST00000586946.1:c.*36_*37delinsCT	ENSP00000465656.1:n.*36_*37delinsCT
ENST00000587837.5:c.*36_*37delinsCT	ENSP00000465081.1:n.*36_*37delinsCT
ENST00000588439.1:n.295_296delinsCT
ENST00000589517.1:c.151_152delinsCT	ENSP00000468447.1:p.Leu51=
NM_001173514.1:c.118_119delinsCT	NP_001166985.1:p.Leu40=
NM_001173515.1:c.118_119delinsCT	NP_001166986.1:p.Leu40=
NM_003332.3:c.151_152delinsCT , LRG_607t1:c.151_152delinsCT	NP_003323.1:p.Leu51=
NM_198125.2:c.151_152delinsCT	NP_937758.1:p.Leu51=
NR_033390.1:n.192_193delinsCT
NM_001173514.2:c.118_119delinsCT	NP_001166985.1:p.Leu40=
NM_001173515.2:c.118_119delinsCT	NP_001166986.1:p.Leu40=
NM_003332.4:c.151_152delinsCT MANE Select	NP_003323.1:p.Leu51=
NM_198125.3:c.151_152delinsCT	NP_937758.1:p.Leu51=
NR_033390.2:n.178_179delinsCT