Canonical Allele Identifier: CA1172569394

Gene: PDE4B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.66092910_66092911delinsCA , CM000663.2:g.66092910_66092911delinsCA	GRCh38
NC_000001.10:g.66558593_66558594delinsCA , CM000663.1:g.66558593_66558594delinsCA	GRCh37
NC_000001.9:g.66331181_66331182delinsCA	NCBI36
NG_029038.1:g.305401_305402delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000341517.9:c.282-154550_282-154549delinsCA MANE Select	ENSP00000342637.4:n.282-154550_282-154549delinsCA
ENST00000329654.8:c.282-154550_282-154549delinsCA	ENSP00000332116.4:n.282-154550_282-154549delinsCA
ENST00000341517.8:c.282-154550_282-154549delinsCA	ENSP00000342637.4:n.282-154550_282-154549delinsCA
ENST00000423207.6:c.236+99768_236+99769delinsCA	ENSP00000392947.2:n.236+99768_236+99769delinsCA
ENST00000526666.1:n.473+44020_473+44021delinsCA
ENST00000531358.1:n.528-19860_528-19859delinsCA
ENST00000532040.1:n.472+29953_472+29954delinsCA
NM_001037340.2:c.236+99768_236+99769delinsCA	NP_001032417.1:n.236+99768_236+99769delinsCA
NM_001037341.1:c.282-154550_282-154549delinsCA	NP_001032418.1:n.282-154550_282-154549delinsCA
NM_001297440.1:c.6-154550_6-154549delinsCA	NP_001284369.1:n.6-154550_6-154549delinsCA
NM_001297441.1:c.56+52202_56+52203delinsCA	NP_001284370.1:n.56+52202_56+52203delinsCA
NM_002600.3:c.282-154550_282-154549delinsCA	NP_002591.2:n.282-154550_282-154549delinsCA
XM_011541565.1:c.17+44020_17+44021delinsCA	XP_011539867.1:n.17+44020_17+44021delinsCA
XM_011541566.1:c.-287-154550_-287-154549delinsCA	XP_011539868.1:n.-287-154550_-287-154549delinsCA
NM_002600.4:c.282-154550_282-154549delinsCA MANE Select	NP_002591.2:n.282-154550_282-154549delinsCA
NM_001037340.3:c.236+99768_236+99769delinsCA	NP_001032417.1:n.236+99768_236+99769delinsCA
NM_001037341.2:c.282-154550_282-154549delinsCA	NP_001032418.1:n.282-154550_282-154549delinsCA
NM_001297440.2:c.6-154550_6-154549delinsCA	NP_001284369.1:n.6-154550_6-154549delinsCA