Canonical Allele Identifier: CA2333879139
Gene: TYROBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35908130A= , CM000681.2:g.35908130A= GRCh38
NC_000019.9:g.36399032A= , CM000681.1:g.36399032A= GRCh37
NC_000019.8:g.41090872A= NCBI36
NG_009304.1:g.5155T= , LRG_607:g.5155T=

Transcript Alleles

HGVS Amino-acid change
ENST00000262629.9:c.61+38T= MANE Select ENSP00000262629.3:n.61+38T=
ENST00000262629.8:c.61+38T= ENSP00000262629.3:n.61+38T=
ENST00000424586.7:c.61+38T= ENSP00000402371.3:n.61+38T=
ENST00000544690.6:c.61+38T= ENSP00000445332.1:n.61+38T=
ENST00000585626.1:n.128+38T=
ENST00000585901.6:c.61+38T= ENSP00000468608.1:n.61+38T=
ENST00000586946.1:c.54+45T= ENSP00000465656.1:n.54+45T=
ENST00000587837.5:c.54+45T= ENSP00000465081.1:n.54+45T=
ENST00000588439.1:n.56+38T=
ENST00000589517.1:c.61+38T= ENSP00000468447.1:n.61+38T=
NM_001173514.1:c.61+38T= NP_001166985.1:n.61+38T=
NM_001173515.1:c.61+38T= NP_001166986.1:n.61+38T=
NM_003332.3:c.61+38T= , LRG_607t1:c.61+38T= NP_003323.1:n.61+38T=
NM_198125.2:c.61+38T= NP_937758.1:n.61+38T=
NR_033390.1:n.135+45T=
NM_001173514.2:c.61+38T= NP_001166985.1:n.61+38T=
NM_001173515.2:c.61+38T= NP_001166986.1:n.61+38T=
NM_003332.4:c.61+38T= MANE Select NP_003323.1:n.61+38T=
NM_198125.3:c.61+38T= NP_937758.1:n.61+38T=
NR_033390.2:n.121+45T=