Canonical Allele Identifier: CA1432845192

Gene: PDE6B PDE6B-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.654232_654233delinsAG , CM000666.2:g.654232_654233delinsAG	GRCh38
NC_000004.11:g.648021_648022delinsAG , CM000666.1:g.648021_648022delinsAG	GRCh37
NC_000004.10:g.638021_638022delinsAG	NCBI36
NG_009839.1:g.33659_33660delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496514.6:c.927+78_927+79delinsAG (PDE6B) MANE Select	ENSP00000420295.1:n.927+78_927+79delinsAG
ENST00000255622.10:c.927+78_927+79delinsAG (PDE6B)	ENSP00000255622.6:n.927+78_927+79delinsAG
ENST00000429163.6:c.90+78_90+79delinsAG (PDE6B)	ENSP00000406334.2:n.90+78_90+79delinsAG
ENST00000465426.5:c.90+78_90+79delinsAG (PDE6B)	ENSP00000418454.1:n.90+78_90+79delinsAG
ENST00000467152.1:n.403_404delinsAG (PDE6B)
ENST00000474251.5:n.456_457delinsAG (PDE6B)
ENST00000476034.5:n.575_576delinsAG (PDE6B)
ENST00000487902.5:c.90+78_90+79delinsAG (PDE6B)	ENSP00000418256.1:n.90+78_90+79delinsAG
ENST00000496514.5:c.927+78_927+79delinsAG (PDE6B)	ENSP00000420295.1:n.927+78_927+79delinsAG
NM_000283.3:c.927+78_927+79delinsAG (PDE6B)	NP_000274.2:n.927+78_927+79delinsAG
NM_001145291.1:c.927+78_927+79delinsAG (PDE6B)	NP_001138763.1:n.927+78_927+79delinsAG
NM_001145292.1:c.90+78_90+79delinsAG (PDE6B)	NP_001138764.1:n.90+78_90+79delinsAG
XM_011513473.1:c.1146+78_1146+79delinsAG (PDE6B)	XP_011511775.1:n.1146+78_1146+79delinsAG
XM_011513474.1:c.1146+78_1146+79delinsAG (PDE6B)	XP_011511776.1:n.1146+78_1146+79delinsAG
XM_011513475.1:c.927+78_927+79delinsAG (PDE6B)	XP_011511777.1:n.927+78_927+79delinsAG
XM_011513476.1:c.1146+78_1146+79delinsAG (PDE6B)	XP_011511778.1:n.1146+78_1146+79delinsAG
XM_011513477.1:c.-393_-392delinsAG (PDE6B)	XP_011511779.1:n.-393_-392delinsAG
XM_011513478.1:c.-736_-735delinsAG (PDE6B)	XP_011511780.1:n.-736_-735delinsAG
XR_246615.2:n.866-20_866-19delinsCT (PDE6B-AS1)
XR_925030.1:n.866-262_866-261delinsCT (PDE6B-AS1)
NM_001350154.1:c.90+78_90+79delinsAG (PDE6B)	NP_001337083.1:n.90+78_90+79delinsAG
NM_001350155.1:c.-114+78_-114+79delinsAG (PDE6B)	NP_001337084.1:n.-114+78_-114+79delinsAG
XM_011513473.3:c.1146+78_1146+79delinsAG (PDE6B)	XP_011511775.1:n.1146+78_1146+79delinsAG
XM_011513474.3:c.1146+78_1146+79delinsAG (PDE6B)	XP_011511776.1:n.1146+78_1146+79delinsAG
XM_011513475.2:c.927+78_927+79delinsAG (PDE6B)	XP_011511777.1:n.927+78_927+79delinsAG
XM_011513476.3:c.1146+78_1146+79delinsAG (PDE6B)	XP_011511778.1:n.1146+78_1146+79delinsAG
XM_011513478.2:c.-736_-735delinsAG (PDE6B)	XP_011511780.1:n.-736_-735delinsAG
XM_017008284.1:c.90+78_90+79delinsAG (PDE6B)	XP_016863773.1:n.90+78_90+79delinsAG
XM_017008285.1:c.90+78_90+79delinsAG (PDE6B)	XP_016863774.1:n.90+78_90+79delinsAG
XM_017008286.1:c.90+78_90+79delinsAG (PDE6B)	XP_016863775.1:n.90+78_90+79delinsAG
XR_001741541.1:n.1108-262_1108-261delinsCT (PDE6B-AS1)
XR_246615.3:n.1108-20_1108-19delinsCT (PDE6B-AS1)
NM_001350154.2:c.90+78_90+79delinsAG (PDE6B)	NP_001337083.1:n.90+78_90+79delinsAG
NM_001350155.2:c.-114+78_-114+79delinsAG (PDE6B)	NP_001337084.1:n.-114+78_-114+79delinsAG
NM_000283.4:c.927+78_927+79delinsAG (PDE6B) MANE Select	NP_000274.3:n.927+78_927+79delinsAG
NM_001145291.2:c.927+78_927+79delinsAG (PDE6B)	NP_001138763.2:n.927+78_927+79delinsAG
NM_001145292.2:c.90+78_90+79delinsAG (PDE6B)	NP_001138764.2:n.90+78_90+79delinsAG
NM_001350154.3:c.90+78_90+79delinsAG (PDE6B)	NP_001337083.1:n.90+78_90+79delinsAG
NM_001350155.3:c.-114+78_-114+79delinsAG (PDE6B)	NP_001337084.1:n.-114+78_-114+79delinsAG
NM_001379246.1:c.90+78_90+79delinsAG (PDE6B)	NP_001366175.1:n.90+78_90+79delinsAG
NM_001379247.1:c.90+78_90+79delinsAG (PDE6B)	NP_001366176.1:n.90+78_90+79delinsAG