Canonical Allele Identifier: CA2760111347

Gene: PDE6B PDE6B-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.654270_654271insAGAT , CM000666.2:g.654270_654271insAGAT	GRCh38
NC_000004.11:g.648059_648060insAGAT , CM000666.1:g.648059_648060insAGAT	GRCh37
NC_000004.10:g.638059_638060insAGAT	NCBI36
NG_009839.1:g.33697_33698insAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496514.6:c.927+116_927+117insAGAT (PDE6B) MANE Select	ENSP00000420295.1:n.927+116_927+117insAGAT
ENST00000255622.10:c.927+116_927+117insAGAT (PDE6B)	ENSP00000255622.6:n.927+116_927+117insAGAT
ENST00000429163.6:c.90+116_90+117insAGAT (PDE6B)	ENSP00000406334.2:n.90+116_90+117insAGAT
ENST00000465426.5:c.90+116_90+117insAGAT (PDE6B)	ENSP00000418454.1:n.90+116_90+117insAGAT
ENST00000467152.1:n.441_442insAGAT (PDE6B)
ENST00000474251.5:n.494_495insAGAT (PDE6B)
ENST00000476034.5:n.613_614insAGAT (PDE6B)
ENST00000487902.5:c.90+116_90+117insAGAT (PDE6B)	ENSP00000418256.1:n.90+116_90+117insAGAT
ENST00000496514.5:c.927+116_927+117insAGAT (PDE6B)	ENSP00000420295.1:n.927+116_927+117insAGAT
NM_000283.3:c.927+116_927+117insAGAT (PDE6B)	NP_000274.2:n.927+116_927+117insAGAT
NM_001145291.1:c.927+116_927+117insAGAT (PDE6B)	NP_001138763.1:n.927+116_927+117insAGAT
NM_001145292.1:c.90+116_90+117insAGAT (PDE6B)	NP_001138764.1:n.90+116_90+117insAGAT
XM_011513473.1:c.1146+116_1146+117insAGAT (PDE6B)	XP_011511775.1:n.1146+116_1146+117insAGAT
XM_011513474.1:c.1146+116_1146+117insAGAT (PDE6B)	XP_011511776.1:n.1146+116_1146+117insAGAT
XM_011513475.1:c.927+116_927+117insAGAT (PDE6B)	XP_011511777.1:n.927+116_927+117insAGAT
XM_011513476.1:c.1146+116_1146+117insAGAT (PDE6B)	XP_011511778.1:n.1146+116_1146+117insAGAT
XM_011513477.1:c.-355_-354insAGAT (PDE6B)	XP_011511779.1:n.-355_-354insAGAT
XM_011513478.1:c.-698_-697insAGAT (PDE6B)	XP_011511780.1:n.-698_-697insAGAT
XR_246615.2:n.866-58_866-57insATCT (PDE6B-AS1)
XR_925030.1:n.866-300_866-299insATCT (PDE6B-AS1)
NM_001350154.1:c.90+116_90+117insAGAT (PDE6B)	NP_001337083.1:n.90+116_90+117insAGAT
NM_001350155.1:c.-114+116_-114+117insAGAT (PDE6B)	NP_001337084.1:n.-114+116_-114+117insAGAT
XM_011513473.3:c.1146+116_1146+117insAGAT (PDE6B)	XP_011511775.1:n.1146+116_1146+117insAGAT
XM_011513474.3:c.1146+116_1146+117insAGAT (PDE6B)	XP_011511776.1:n.1146+116_1146+117insAGAT
XM_011513475.2:c.927+116_927+117insAGAT (PDE6B)	XP_011511777.1:n.927+116_927+117insAGAT
XM_011513476.3:c.1146+116_1146+117insAGAT (PDE6B)	XP_011511778.1:n.1146+116_1146+117insAGAT
XM_011513478.2:c.-698_-697insAGAT (PDE6B)	XP_011511780.1:n.-698_-697insAGAT
XM_017008284.1:c.90+116_90+117insAGAT (PDE6B)	XP_016863773.1:n.90+116_90+117insAGAT
XM_017008285.1:c.90+116_90+117insAGAT (PDE6B)	XP_016863774.1:n.90+116_90+117insAGAT
XM_017008286.1:c.90+116_90+117insAGAT (PDE6B)	XP_016863775.1:n.90+116_90+117insAGAT
XR_001741541.1:n.1108-300_1108-299insATCT (PDE6B-AS1)
XR_246615.3:n.1108-58_1108-57insATCT (PDE6B-AS1)
NM_001350154.2:c.90+116_90+117insAGAT (PDE6B)	NP_001337083.1:n.90+116_90+117insAGAT
NM_001350155.2:c.-114+116_-114+117insAGAT (PDE6B)	NP_001337084.1:n.-114+116_-114+117insAGAT
NM_000283.4:c.927+116_927+117insAGAT (PDE6B) MANE Select	NP_000274.3:n.927+116_927+117insAGAT
NM_001145291.2:c.927+116_927+117insAGAT (PDE6B)	NP_001138763.2:n.927+116_927+117insAGAT
NM_001145292.2:c.90+116_90+117insAGAT (PDE6B)	NP_001138764.2:n.90+116_90+117insAGAT
NM_001350154.3:c.90+116_90+117insAGAT (PDE6B)	NP_001337083.1:n.90+116_90+117insAGAT
NM_001350155.3:c.-114+116_-114+117insAGAT (PDE6B)	NP_001337084.1:n.-114+116_-114+117insAGAT
NM_001379246.1:c.90+116_90+117insAGAT (PDE6B)	NP_001366175.1:n.90+116_90+117insAGAT
NM_001379247.1:c.90+116_90+117insAGAT (PDE6B)	NP_001366176.1:n.90+116_90+117insAGAT