Canonical Allele Identifier: CA1432854476

Gene: PDE6B

Linked Data

• dbSNP Id: rs1737621862
• gnomAD v4: 4-664982-C-CAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.664982_664983insAGG , CM000666.2:g.664982_664983insAGG	GRCh38
NC_000004.11:g.658771_658772insAGG , CM000666.1:g.658771_658772insAGG	GRCh37
NC_000004.10:g.648771_648772insAGG	NCBI36
NG_009839.1:g.44409_44410insAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496514.6:c.2193+38_2193+39insAGG MANE Select	ENSP00000420295.1:n.2193+38_2193+39insAGG
ENST00000255622.10:c.2193+38_2193+39insAGG	ENSP00000255622.6:n.2193+38_2193+39insAGG
ENST00000429163.6:c.1356+38_1356+39insAGG	ENSP00000406334.2:n.1356+38_1356+39insAGG
ENST00000461490.1:c.35+38_35+39insAGG
ENST00000471824.6:c.273+38_273+39insAGG	ENSP00000417852.2:n.273+38_273+39insAGG
ENST00000496514.5:c.2193+38_2193+39insAGG	ENSP00000420295.1:n.2193+38_2193+39insAGG
NM_000283.3:c.2193+38_2193+39insAGG	NP_000274.2:n.2193+38_2193+39insAGG
NM_001145291.1:c.2193+38_2193+39insAGG	NP_001138763.1:n.2193+38_2193+39insAGG
NM_001145292.1:c.1356+38_1356+39insAGG	NP_001138764.1:n.1356+38_1356+39insAGG
XM_011513473.1:c.2412+38_2412+39insAGG	XP_011511775.1:n.2412+38_2412+39insAGG
XM_011513474.1:c.2412+38_2412+39insAGG	XP_011511776.1:n.2412+38_2412+39insAGG
XM_011513475.1:c.2193+38_2193+39insAGG	XP_011511777.1:n.2193+38_2193+39insAGG
XM_011513476.1:c.2412+38_2412+39insAGG	XP_011511778.1:n.2412+38_2412+39insAGG
XM_011513477.1:c.1398+38_1398+39insAGG	XP_011511779.1:n.1398+38_1398+39insAGG
XM_011513478.1:c.1122+38_1122+39insAGG	XP_011511780.1:n.1122+38_1122+39insAGG
NM_001350154.1:c.1356+38_1356+39insAGG	NP_001337083.1:n.1356+38_1356+39insAGG
NM_001350155.1:c.1038+38_1038+39insAGG	NP_001337084.1:n.1038+38_1038+39insAGG
XM_011513473.3:c.2412+38_2412+39insAGG	XP_011511775.1:n.2412+38_2412+39insAGG
XM_011513474.3:c.2412+38_2412+39insAGG	XP_011511776.1:n.2412+38_2412+39insAGG
XM_011513475.2:c.2193+38_2193+39insAGG	XP_011511777.1:n.2193+38_2193+39insAGG
XM_011513476.3:c.2412+38_2412+39insAGG	XP_011511778.1:n.2412+38_2412+39insAGG
XM_011513478.2:c.1122+38_1122+39insAGG	XP_011511780.1:n.1122+38_1122+39insAGG
XM_017008284.1:c.1356+38_1356+39insAGG	XP_016863773.1:n.1356+38_1356+39insAGG
XM_017008285.1:c.1356+38_1356+39insAGG	XP_016863774.1:n.1356+38_1356+39insAGG
XM_017008286.1:c.1356+38_1356+39insAGG	XP_016863775.1:n.1356+38_1356+39insAGG
NM_001350154.2:c.1356+38_1356+39insAGG	NP_001337083.1:n.1356+38_1356+39insAGG
NM_001350155.2:c.1038+38_1038+39insAGG	NP_001337084.1:n.1038+38_1038+39insAGG
NM_000283.4:c.2193+38_2193+39insAGG MANE Select	NP_000274.3:n.2193+38_2193+39insAGG
NM_001145291.2:c.2193+38_2193+39insAGG	NP_001138763.2:n.2193+38_2193+39insAGG
NM_001145292.2:c.1356+38_1356+39insAGG	NP_001138764.2:n.1356+38_1356+39insAGG
NM_001350154.3:c.1356+38_1356+39insAGG	NP_001337083.1:n.1356+38_1356+39insAGG
NM_001350155.3:c.1038+38_1038+39insAGG	NP_001337084.1:n.1038+38_1038+39insAGG
NM_001379246.1:c.1356+38_1356+39insAGG	NP_001366175.1:n.1356+38_1356+39insAGG
NM_001379247.1:c.1356+38_1356+39insAGG	NP_001366176.1:n.1356+38_1356+39insAGG