Canonical Allele Identifier: CA2322438335

Gene: PDE4A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10457643T= , CM000681.2:g.10457643T=	GRCh38
NC_000019.9:g.10568319T= , CM000681.1:g.10568319T=	GRCh37
NC_000019.8:g.10429319T=	NCBI36
NG_029594.1:g.45871T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380702.7:c.878-236T= MANE Select	ENSP00000370078.3:n.878-236T=
ENST00000293683.9:c.800-236T=	ENSP00000293683.4:n.800-236T=
ENST00000344979.7:c.161-236T=	ENSP00000341007.2:n.161-236T=
ENST00000380702.6:c.878-236T=	ENSP00000370078.3:n.878-236T=
ENST00000440014.6:c.695-236T=	ENSP00000394754.1:n.695-236T=
ENST00000586275.1:n.141-236T=
ENST00000589073.1:c.160+2721T=	ENSP00000465792.1:n.160+2721T=
ENST00000591971.5:c.206-236T=	ENSP00000467137.1:n.206-236T=
ENST00000592685.5:c.812-236T=	ENSP00000468507.1:n.812-236T=
NM_001111307.1:c.878-236T=	NP_001104777.1:n.878-236T=
NM_001111308.1:c.800-236T=	NP_001104778.1:n.800-236T=
NM_001111309.1:c.695-236T=	NP_001104779.1:n.695-236T=
NM_001243121.1:c.812-236T=	NP_001230050.1:n.812-236T=
NM_006202.2:c.161-236T=	NP_006193.1:n.161-236T=
XM_005259933.2:c.-166-7T=	XP_005259990.1:n.-166-7T=
XM_011528054.1:c.812-236T=	XP_011526356.1:n.812-236T=
XM_011528055.1:c.878-236T=	XP_011526357.1:n.878-236T=
XM_011528055.3:c.878-236T=	XP_011526357.1:n.878-236T=
XM_017026865.2:c.875-236T=	XP_016882354.1:n.875-236T=
XM_024451534.1:c.-166-7T=	XP_024307302.1:n.-166-7T=
NM_001111307.2:c.878-236T= MANE Select	NP_001104777.1:n.878-236T=
NM_006202.3:c.161-236T=	NP_006193.1:n.161-236T=
NM_001243121.2:c.812-236T=	NP_001230050.1:n.812-236T=