Canonical Allele Identifier: CA1172569385

Gene: PDE4B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.66092889_66092892delinsAGAG , CM000663.2:g.66092889_66092892delinsAGAG	GRCh38
NC_000001.10:g.66558572_66558575delinsAGAG , CM000663.1:g.66558572_66558575delinsAGAG	GRCh37
NC_000001.9:g.66331160_66331163delinsAGAG	NCBI36
NG_029038.1:g.305380_305383delinsAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341517.9:c.282-154571_282-154568delinsAGAG MANE Select	ENSP00000342637.4:n.282-154571_282-154568delinsAGAG
ENST00000329654.8:c.282-154571_282-154568delinsAGAG	ENSP00000332116.4:n.282-154571_282-154568delinsAGAG
ENST00000341517.8:c.282-154571_282-154568delinsAGAG	ENSP00000342637.4:n.282-154571_282-154568delinsAGAG
ENST00000423207.6:c.236+99747_236+99750delinsAGAG	ENSP00000392947.2:n.236+99747_236+99750delinsAGAG
ENST00000526666.1:n.473+43999_473+44002delinsAGAG
ENST00000531358.1:n.528-19881_528-19878delinsAGAG
ENST00000532040.1:n.472+29932_472+29935delinsAGAG
NM_001037340.2:c.236+99747_236+99750delinsAGAG	NP_001032417.1:n.236+99747_236+99750delinsAGAG
NM_001037341.1:c.282-154571_282-154568delinsAGAG	NP_001032418.1:n.282-154571_282-154568delinsAGAG
NM_001297440.1:c.6-154571_6-154568delinsAGAG	NP_001284369.1:n.6-154571_6-154568delinsAGAG
NM_001297441.1:c.56+52181_56+52184delinsAGAG	NP_001284370.1:n.56+52181_56+52184delinsAGAG
NM_002600.3:c.282-154571_282-154568delinsAGAG	NP_002591.2:n.282-154571_282-154568delinsAGAG
XM_011541565.1:c.17+43999_17+44002delinsAGAG	XP_011539867.1:n.17+43999_17+44002delinsAGAG
XM_011541566.1:c.-287-154571_-287-154568delinsAGAG	XP_011539868.1:n.-287-154571_-287-154568delinsAGAG
NM_002600.4:c.282-154571_282-154568delinsAGAG MANE Select	NP_002591.2:n.282-154571_282-154568delinsAGAG
NM_001037340.3:c.236+99747_236+99750delinsAGAG	NP_001032417.1:n.236+99747_236+99750delinsAGAG
NM_001037341.2:c.282-154571_282-154568delinsAGAG	NP_001032418.1:n.282-154571_282-154568delinsAGAG
NM_001297440.2:c.6-154571_6-154568delinsAGAG	NP_001284369.1:n.6-154571_6-154568delinsAGAG