Canonical Allele Identifier: CA1002679975

Gene: PDE4B

Linked Data

• dbSNP Id: rs1645054079
• gnomAD v3: 1-66093035-CTT-C
• gnomAD v4: 1-66093035-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.66093037_66093038del , CM000663.2:g.66093037_66093038del	GRCh38
NC_000001.10:g.66558720_66558721del , CM000663.1:g.66558720_66558721del	GRCh37
NC_000001.9:g.66331308_66331309del	NCBI36
NG_029038.1:g.305528_305529del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341517.9:c.282-154423_282-154422del MANE Select	ENSP00000342637.4:n.282-154423_282-154422del
ENST00000329654.8:c.282-154423_282-154422del	ENSP00000332116.4:n.282-154423_282-154422del
ENST00000341517.8:c.282-154423_282-154422del	ENSP00000342637.4:n.282-154423_282-154422del
ENST00000423207.6:c.236+99895_236+99896del	ENSP00000392947.2:n.236+99895_236+99896del
ENST00000526666.1:n.473+44147_473+44148del
ENST00000531358.1:n.528-19733_528-19732del
ENST00000532040.1:n.472+30080_472+30081del
NM_001037340.2:c.236+99895_236+99896del	NP_001032417.1:n.236+99895_236+99896del
NM_001037341.1:c.282-154423_282-154422del	NP_001032418.1:n.282-154423_282-154422del
NM_001297440.1:c.6-154423_6-154422del	NP_001284369.1:n.6-154423_6-154422del
NM_001297441.1:c.56+52329_56+52330del	NP_001284370.1:n.56+52329_56+52330del
NM_002600.3:c.282-154423_282-154422del	NP_002591.2:n.282-154423_282-154422del
XM_011541565.1:c.17+44147_17+44148del	XP_011539867.1:n.17+44147_17+44148del
XM_011541566.1:c.-287-154423_-287-154422del	XP_011539868.1:n.-287-154423_-287-154422del
NM_002600.4:c.282-154423_282-154422del MANE Select	NP_002591.2:n.282-154423_282-154422del
NM_001037340.3:c.236+99895_236+99896del	NP_001032417.1:n.236+99895_236+99896del
NM_001037341.2:c.282-154423_282-154422del	NP_001032418.1:n.282-154423_282-154422del
NM_001297440.2:c.6-154423_6-154422del	NP_001284369.1:n.6-154423_6-154422del