Canonical Allele Identifier: CA2760111391

Gene: PDE6B PDE6B-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.654313_654314insAG , CM000666.2:g.654313_654314insAG	GRCh38
NC_000004.11:g.648102_648103insAG , CM000666.1:g.648102_648103insAG	GRCh37
NC_000004.10:g.638102_638103insAG	NCBI36
NG_009839.1:g.33740_33741insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496514.6:c.927+159_927+160insAG (PDE6B) MANE Select	ENSP00000420295.1:n.927+159_927+160insAG
ENST00000255622.10:c.927+159_927+160insAG (PDE6B)	ENSP00000255622.6:n.927+159_927+160insAG
ENST00000429163.6:c.90+159_90+160insAG (PDE6B)	ENSP00000406334.2:n.90+159_90+160insAG
ENST00000465426.5:c.90+159_90+160insAG (PDE6B)	ENSP00000418454.1:n.90+159_90+160insAG
ENST00000467152.1:n.484_485insAG (PDE6B)
ENST00000476034.5:n.656_657insAG (PDE6B)
ENST00000487902.5:c.90+159_90+160insAG (PDE6B)	ENSP00000418256.1:n.90+159_90+160insAG
ENST00000496514.5:c.927+159_927+160insAG (PDE6B)	ENSP00000420295.1:n.927+159_927+160insAG
NM_000283.3:c.927+159_927+160insAG (PDE6B)	NP_000274.2:n.927+159_927+160insAG
NM_001145291.1:c.927+159_927+160insAG (PDE6B)	NP_001138763.1:n.927+159_927+160insAG
NM_001145292.1:c.90+159_90+160insAG (PDE6B)	NP_001138764.1:n.90+159_90+160insAG
XM_011513473.1:c.1146+159_1146+160insAG (PDE6B)	XP_011511775.1:n.1146+159_1146+160insAG
XM_011513474.1:c.1146+159_1146+160insAG (PDE6B)	XP_011511776.1:n.1146+159_1146+160insAG
XM_011513475.1:c.927+159_927+160insAG (PDE6B)	XP_011511777.1:n.927+159_927+160insAG
XM_011513476.1:c.1146+159_1146+160insAG (PDE6B)	XP_011511778.1:n.1146+159_1146+160insAG
XM_011513477.1:c.-312_-311insAG (PDE6B)	XP_011511779.1:n.-312_-311insAG
XM_011513478.1:c.-655_-654insAG (PDE6B)	XP_011511780.1:n.-655_-654insAG
XR_246615.2:n.866-101_866-100insCT (PDE6B-AS1)
XR_925030.1:n.866-343_866-342insCT (PDE6B-AS1)
NM_001350154.1:c.90+159_90+160insAG (PDE6B)	NP_001337083.1:n.90+159_90+160insAG
NM_001350155.1:c.-114+159_-114+160insAG (PDE6B)	NP_001337084.1:n.-114+159_-114+160insAG
XM_011513473.3:c.1146+159_1146+160insAG (PDE6B)	XP_011511775.1:n.1146+159_1146+160insAG
XM_011513474.3:c.1146+159_1146+160insAG (PDE6B)	XP_011511776.1:n.1146+159_1146+160insAG
XM_011513475.2:c.927+159_927+160insAG (PDE6B)	XP_011511777.1:n.927+159_927+160insAG
XM_011513476.3:c.1146+159_1146+160insAG (PDE6B)	XP_011511778.1:n.1146+159_1146+160insAG
XM_011513478.2:c.-655_-654insAG (PDE6B)	XP_011511780.1:n.-655_-654insAG
XM_017008284.1:c.90+159_90+160insAG (PDE6B)	XP_016863773.1:n.90+159_90+160insAG
XM_017008285.1:c.90+159_90+160insAG (PDE6B)	XP_016863774.1:n.90+159_90+160insAG
XM_017008286.1:c.90+159_90+160insAG (PDE6B)	XP_016863775.1:n.90+159_90+160insAG
XR_001741541.1:n.1108-343_1108-342insCT (PDE6B-AS1)
XR_246615.3:n.1108-101_1108-100insCT (PDE6B-AS1)
NM_001350154.2:c.90+159_90+160insAG (PDE6B)	NP_001337083.1:n.90+159_90+160insAG
NM_001350155.2:c.-114+159_-114+160insAG (PDE6B)	NP_001337084.1:n.-114+159_-114+160insAG
NM_000283.4:c.927+159_927+160insAG (PDE6B) MANE Select	NP_000274.3:n.927+159_927+160insAG
NM_001145291.2:c.927+159_927+160insAG (PDE6B)	NP_001138763.2:n.927+159_927+160insAG
NM_001145292.2:c.90+159_90+160insAG (PDE6B)	NP_001138764.2:n.90+159_90+160insAG
NM_001350154.3:c.90+159_90+160insAG (PDE6B)	NP_001337083.1:n.90+159_90+160insAG
NM_001350155.3:c.-114+159_-114+160insAG (PDE6B)	NP_001337084.1:n.-114+159_-114+160insAG
NM_001379246.1:c.90+159_90+160insAG (PDE6B)	NP_001366175.1:n.90+159_90+160insAG
NM_001379247.1:c.90+159_90+160insAG (PDE6B)	NP_001366176.1:n.90+159_90+160insAG