Canonical Allele Identifier: CA1172569454

Gene: PDE4B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.66093045_66093046delinsAG , CM000663.2:g.66093045_66093046delinsAG	GRCh38
NC_000001.10:g.66558728_66558729delinsAG , CM000663.1:g.66558728_66558729delinsAG	GRCh37
NC_000001.9:g.66331316_66331317delinsAG	NCBI36
NG_029038.1:g.305536_305537delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000341517.9:c.282-154415_282-154414delinsAG MANE Select	ENSP00000342637.4:n.282-154415_282-154414delinsAG
ENST00000329654.8:c.282-154415_282-154414delinsAG	ENSP00000332116.4:n.282-154415_282-154414delinsAG
ENST00000341517.8:c.282-154415_282-154414delinsAG	ENSP00000342637.4:n.282-154415_282-154414delinsAG
ENST00000423207.6:c.236+99903_236+99904delinsAG	ENSP00000392947.2:n.236+99903_236+99904delinsAG
ENST00000526666.1:n.473+44155_473+44156delinsAG
ENST00000531358.1:n.528-19725_528-19724delinsAG
ENST00000532040.1:n.472+30088_472+30089delinsAG
NM_001037340.2:c.236+99903_236+99904delinsAG	NP_001032417.1:n.236+99903_236+99904delinsAG
NM_001037341.1:c.282-154415_282-154414delinsAG	NP_001032418.1:n.282-154415_282-154414delinsAG
NM_001297440.1:c.6-154415_6-154414delinsAG	NP_001284369.1:n.6-154415_6-154414delinsAG
NM_001297441.1:c.56+52337_56+52338delinsAG	NP_001284370.1:n.56+52337_56+52338delinsAG
NM_002600.3:c.282-154415_282-154414delinsAG	NP_002591.2:n.282-154415_282-154414delinsAG
XM_011541565.1:c.17+44155_17+44156delinsAG	XP_011539867.1:n.17+44155_17+44156delinsAG
XM_011541566.1:c.-287-154415_-287-154414delinsAG	XP_011539868.1:n.-287-154415_-287-154414delinsAG
NM_002600.4:c.282-154415_282-154414delinsAG MANE Select	NP_002591.2:n.282-154415_282-154414delinsAG
NM_001037340.3:c.236+99903_236+99904delinsAG	NP_001032417.1:n.236+99903_236+99904delinsAG
NM_001037341.2:c.282-154415_282-154414delinsAG	NP_001032418.1:n.282-154415_282-154414delinsAG
NM_001297440.2:c.6-154415_6-154414delinsAG	NP_001284369.1:n.6-154415_6-154414delinsAG