Canonical Allele Identifier: CA2760112484

Gene: PDE6B

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.660763_660764del , CM000666.2:g.660763_660764del	GRCh38
NC_000004.11:g.654552_654553del , CM000666.1:g.654552_654553del	GRCh37
NC_000004.10:g.644552_644553del	NCBI36
NG_009839.1:g.40190_40191del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496514.6:c.1614+150_1614+151del MANE Select	ENSP00000420295.1:n.1614+150_1614+151del
ENST00000255622.10:c.1614+150_1614+151del	ENSP00000255622.6:n.1614+150_1614+151del
ENST00000429163.6:c.777+150_777+151del	ENSP00000406334.2:n.777+150_777+151del
ENST00000496514.5:c.1614+150_1614+151del	ENSP00000420295.1:n.1614+150_1614+151del
NM_000283.3:c.1614+150_1614+151del	NP_000274.2:n.1614+150_1614+151del
NM_001145291.1:c.1614+150_1614+151del	NP_001138763.1:n.1614+150_1614+151del
NM_001145292.1:c.777+150_777+151del	NP_001138764.1:n.777+150_777+151del
XM_011513473.1:c.1833+150_1833+151del	XP_011511775.1:n.1833+150_1833+151del
XM_011513474.1:c.1833+150_1833+151del	XP_011511776.1:n.1833+150_1833+151del
XM_011513475.1:c.1614+150_1614+151del	XP_011511777.1:n.1614+150_1614+151del
XM_011513476.1:c.1833+150_1833+151del	XP_011511778.1:n.1833+150_1833+151del
XM_011513477.1:c.819+150_819+151del	XP_011511779.1:n.819+150_819+151del
XM_011513478.1:c.543+150_543+151del	XP_011511780.1:n.543+150_543+151del
NM_001350154.1:c.777+150_777+151del	NP_001337083.1:n.777+150_777+151del
NM_001350155.1:c.459+150_459+151del	NP_001337084.1:n.459+150_459+151del
XM_011513473.3:c.1833+150_1833+151del	XP_011511775.1:n.1833+150_1833+151del
XM_011513474.3:c.1833+150_1833+151del	XP_011511776.1:n.1833+150_1833+151del
XM_011513475.2:c.1614+150_1614+151del	XP_011511777.1:n.1614+150_1614+151del
XM_011513476.3:c.1833+150_1833+151del	XP_011511778.1:n.1833+150_1833+151del
XM_011513478.2:c.543+150_543+151del	XP_011511780.1:n.543+150_543+151del
XM_017008284.1:c.777+150_777+151del	XP_016863773.1:n.777+150_777+151del
XM_017008285.1:c.777+150_777+151del	XP_016863774.1:n.777+150_777+151del
XM_017008286.1:c.777+150_777+151del	XP_016863775.1:n.777+150_777+151del
NM_001350154.2:c.777+150_777+151del	NP_001337083.1:n.777+150_777+151del
NM_001350155.2:c.459+150_459+151del	NP_001337084.1:n.459+150_459+151del
NM_000283.4:c.1614+150_1614+151del MANE Select	NP_000274.3:n.1614+150_1614+151del
NM_001145291.2:c.1614+150_1614+151del	NP_001138763.2:n.1614+150_1614+151del
NM_001145292.2:c.777+150_777+151del	NP_001138764.2:n.777+150_777+151del
NM_001350154.3:c.777+150_777+151del	NP_001337083.1:n.777+150_777+151del
NM_001350155.3:c.459+150_459+151del	NP_001337084.1:n.459+150_459+151del
NM_001379246.1:c.777+150_777+151del	NP_001366175.1:n.777+150_777+151del
NM_001379247.1:c.777+150_777+151del	NP_001366176.1:n.777+150_777+151del