Canonical Allele Identifier: CA2669420393

Gene: PDE6B

Linked Data

• gnomAD v4: 4-665001-C-CCGGGCGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.665006_665013dup , CM000666.2:g.665006_665013dup	GRCh38
NC_000004.11:g.658795_658802dup , CM000666.1:g.658795_658802dup	GRCh37
NC_000004.10:g.648795_648802dup	NCBI36
NG_009839.1:g.44433_44440dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496514.6:c.2193+62_2193+69dup MANE Select	ENSP00000420295.1:n.2193+62_2193+69dup
ENST00000255622.10:c.2193+62_2193+69dup	ENSP00000255622.6:n.2193+62_2193+69dup
ENST00000429163.6:c.1356+62_1356+69dup	ENSP00000406334.2:n.1356+62_1356+69dup
ENST00000461490.1:c.35+62_35+69dup
ENST00000471824.6:c.273+62_273+69dup	ENSP00000417852.2:n.273+62_273+69dup
ENST00000496514.5:c.2193+62_2193+69dup	ENSP00000420295.1:n.2193+62_2193+69dup
NM_000283.3:c.2193+62_2193+69dup	NP_000274.2:n.2193+62_2193+69dup
NM_001145291.1:c.2193+62_2193+69dup	NP_001138763.1:n.2193+62_2193+69dup
NM_001145292.1:c.1356+62_1356+69dup	NP_001138764.1:n.1356+62_1356+69dup
XM_011513473.1:c.2412+62_2412+69dup	XP_011511775.1:n.2412+62_2412+69dup
XM_011513474.1:c.2412+62_2412+69dup	XP_011511776.1:n.2412+62_2412+69dup
XM_011513475.1:c.2193+62_2193+69dup	XP_011511777.1:n.2193+62_2193+69dup
XM_011513476.1:c.2412+62_2412+69dup	XP_011511778.1:n.2412+62_2412+69dup
XM_011513477.1:c.1398+62_1398+69dup	XP_011511779.1:n.1398+62_1398+69dup
XM_011513478.1:c.1122+62_1122+69dup	XP_011511780.1:n.1122+62_1122+69dup
NM_001350154.1:c.1356+62_1356+69dup	NP_001337083.1:n.1356+62_1356+69dup
NM_001350155.1:c.1038+62_1038+69dup	NP_001337084.1:n.1038+62_1038+69dup
XM_011513473.3:c.2412+62_2412+69dup	XP_011511775.1:n.2412+62_2412+69dup
XM_011513474.3:c.2412+62_2412+69dup	XP_011511776.1:n.2412+62_2412+69dup
XM_011513475.2:c.2193+62_2193+69dup	XP_011511777.1:n.2193+62_2193+69dup
XM_011513476.3:c.2412+62_2412+69dup	XP_011511778.1:n.2412+62_2412+69dup
XM_011513478.2:c.1122+62_1122+69dup	XP_011511780.1:n.1122+62_1122+69dup
XM_017008284.1:c.1356+62_1356+69dup	XP_016863773.1:n.1356+62_1356+69dup
XM_017008285.1:c.1356+62_1356+69dup	XP_016863774.1:n.1356+62_1356+69dup
XM_017008286.1:c.1356+62_1356+69dup	XP_016863775.1:n.1356+62_1356+69dup
NM_001350154.2:c.1356+62_1356+69dup	NP_001337083.1:n.1356+62_1356+69dup
NM_001350155.2:c.1038+62_1038+69dup	NP_001337084.1:n.1038+62_1038+69dup
NM_000283.4:c.2193+62_2193+69dup MANE Select	NP_000274.3:n.2193+62_2193+69dup
NM_001145291.2:c.2193+62_2193+69dup	NP_001138763.2:n.2193+62_2193+69dup
NM_001145292.2:c.1356+62_1356+69dup	NP_001138764.2:n.1356+62_1356+69dup
NM_001350154.3:c.1356+62_1356+69dup	NP_001337083.1:n.1356+62_1356+69dup
NM_001350155.3:c.1038+62_1038+69dup	NP_001337084.1:n.1038+62_1038+69dup
NM_001379246.1:c.1356+62_1356+69dup	NP_001366175.1:n.1356+62_1356+69dup
NM_001379247.1:c.1356+62_1356+69dup	NP_001366176.1:n.1356+62_1356+69dup