Canonical Allele Identifier: CA1172569443

Gene: PDE4B

Linked Data

• dbSNP Id: rs1645053812

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.66093023_66093027dup , CM000663.2:g.66093023_66093027dup	GRCh38
NC_000001.10:g.66558706_66558710dup , CM000663.1:g.66558706_66558710dup	GRCh37
NC_000001.9:g.66331294_66331298dup	NCBI36
NG_029038.1:g.305514_305518dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000341517.9:c.282-154437_282-154433dup MANE Select	ENSP00000342637.4:n.282-154437_282-154433...
ENST00000329654.8:c.282-154437_282-154433dup	ENSP00000332116.4:n.282-154437_282-154433...
ENST00000341517.8:c.282-154437_282-154433dup	ENSP00000342637.4:n.282-154437_282-154433...
ENST00000423207.6:c.236+99881_236+99885dup	ENSP00000392947.2:n.236+99881_236+99885du...
ENST00000526666.1:n.473+44133_473+44137dup
ENST00000531358.1:n.528-19747_528-19743dup
ENST00000532040.1:n.472+30066_472+30070dup
NM_001037340.2:c.236+99881_236+99885dup	NP_001032417.1:n.236+99881_236+99885dup
NM_001037341.1:c.282-154437_282-154433dup	NP_001032418.1:n.282-154437_282-154433dup...
NM_001297440.1:c.6-154437_6-154433dup	NP_001284369.1:n.6-154437_6-154433dup
NM_001297441.1:c.56+52315_56+52319dup	NP_001284370.1:n.56+52315_56+52319dup
NM_002600.3:c.282-154437_282-154433dup	NP_002591.2:n.282-154437_282-154433dup
XM_011541565.1:c.17+44133_17+44137dup	XP_011539867.1:n.17+44133_17+44137dup
XM_011541566.1:c.-287-154437_-287-154433dup	XP_011539868.1:n.-287-154437_-287-154433d...
NM_002600.4:c.282-154437_282-154433dup MANE Select	NP_002591.2:n.282-154437_282-154433dup
NM_001037340.3:c.236+99881_236+99885dup	NP_001032417.1:n.236+99881_236+99885dup
NM_001037341.2:c.282-154437_282-154433dup	NP_001032418.1:n.282-154437_282-154433dup...
NM_001297440.2:c.6-154437_6-154433dup	NP_001284369.1:n.6-154437_6-154433dup