Canonical Allele Identifier: CA2333879145

Gene: TYROBP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35908137_35908138delinsCG , CM000681.2:g.35908137_35908138delinsCG	GRCh38
NC_000019.9:g.36399039_36399040delinsCG , CM000681.1:g.36399039_36399040delinsCG	GRCh37
NC_000019.8:g.41090879_41090880delinsCG	NCBI36
NG_009304.1:g.5147_5148delinsCG , LRG_607:g.5147_5148delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000262629.9:c.61+30_61+31delinsCG MANE Select	ENSP00000262629.3:n.61+30_61+31delinsCG
ENST00000262629.8:c.61+30_61+31delinsCG	ENSP00000262629.3:n.61+30_61+31delinsCG
ENST00000424586.7:c.61+30_61+31delinsCG	ENSP00000402371.3:n.61+30_61+31delinsCG
ENST00000544690.6:c.61+30_61+31delinsCG	ENSP00000445332.1:n.61+30_61+31delinsCG
ENST00000585626.1:n.128+30_128+31delinsCG
ENST00000585901.6:c.61+30_61+31delinsCG	ENSP00000468608.1:n.61+30_61+31delinsCG
ENST00000586946.1:c.54+37_54+38delinsCG	ENSP00000465656.1:n.54+37_54+38delinsCG
ENST00000587837.5:c.54+37_54+38delinsCG	ENSP00000465081.1:n.54+37_54+38delinsCG
ENST00000588439.1:n.56+30_56+31delinsCG
ENST00000589517.1:c.61+30_61+31delinsCG	ENSP00000468447.1:n.61+30_61+31delinsCG
NM_001173514.1:c.61+30_61+31delinsCG	NP_001166985.1:n.61+30_61+31delinsCG
NM_001173515.1:c.61+30_61+31delinsCG	NP_001166986.1:n.61+30_61+31delinsCG
NM_003332.3:c.61+30_61+31delinsCG , LRG_607t1:c.61+30_61+31delinsCG	NP_003323.1:n.61+30_61+31delinsCG
NM_198125.2:c.61+30_61+31delinsCG	NP_937758.1:n.61+30_61+31delinsCG
NR_033390.1:n.135+37_135+38delinsCG
NM_001173514.2:c.61+30_61+31delinsCG	NP_001166985.1:n.61+30_61+31delinsCG
NM_001173515.2:c.61+30_61+31delinsCG	NP_001166986.1:n.61+30_61+31delinsCG
NM_003332.4:c.61+30_61+31delinsCG MANE Select	NP_003323.1:n.61+30_61+31delinsCG
NM_198125.3:c.61+30_61+31delinsCG	NP_937758.1:n.61+30_61+31delinsCG
NR_033390.2:n.121+37_121+38delinsCG