Canonical Allele Identifier: CA2582385042

Gene: PDE4A

Linked Data

• gnomAD v4: 19-10457674-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10457679del , CM000681.2:g.10457679del	GRCh38
NC_000019.9:g.10568355del , CM000681.1:g.10568355del	GRCh37
NC_000019.8:g.10429355del	NCBI36
NG_029594.1:g.45907del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380702.7:c.878-200del MANE Select	ENSP00000370078.3:n.878-200del
ENST00000293683.9:c.800-200del	ENSP00000293683.4:n.800-200del
ENST00000344979.7:c.161-200del	ENSP00000341007.2:n.161-200del
ENST00000380702.6:c.878-200del	ENSP00000370078.3:n.878-200del
ENST00000440014.6:c.695-200del	ENSP00000394754.1:n.695-200del
ENST00000586275.1:n.141-200del
ENST00000589073.1:c.160+2757del	ENSP00000465792.1:n.160+2757del
ENST00000591971.5:c.206-200del	ENSP00000467137.1:n.206-200del
ENST00000592685.5:c.812-200del	ENSP00000468507.1:n.812-200del
NM_001111307.1:c.878-200del	NP_001104777.1:n.878-200del
NM_001111308.1:c.800-200del	NP_001104778.1:n.800-200del
NM_001111309.1:c.695-200del	NP_001104779.1:n.695-200del
NM_001243121.1:c.812-200del	NP_001230050.1:n.812-200del
NM_006202.2:c.161-200del	NP_006193.1:n.161-200del
XM_005259933.2:c.-137del	XP_005259990.1:n.-137del
XM_011528054.1:c.812-200del	XP_011526356.1:n.812-200del
XM_011528055.1:c.878-200del	XP_011526357.1:n.878-200del
XM_011528055.3:c.878-200del	XP_011526357.1:n.878-200del
XM_017026865.2:c.875-200del	XP_016882354.1:n.875-200del
XM_024451534.1:c.-137del	XP_024307302.1:n.-137del
NM_001111307.2:c.878-200del MANE Select	NP_001104777.1:n.878-200del
NM_006202.3:c.161-200del	NP_006193.1:n.161-200del
NM_001243121.2:c.812-200del	NP_001230050.1:n.812-200del