Canonical Allele Identifier: CA1549229318

Gene: PDE4D

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.59215824G= , CM000667.2:g.59215824G=	GRCh38
NC_000005.9:g.58511650G= , CM000667.1:g.58511650G=	GRCh37
NC_000005.8:g.58547407G=	NCBI36
NG_027957.1:g.1277276C=
NG_027957.2:g.1313506C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507116.6:c.408C=	ENSP00000424852.1:p.Asp136=
ENST00000340635.11:c.600C= MANE Select	ENSP00000345502.6:p.Asp200=
ENST00000636120.1:c.270C=	ENSP00000490821.1:p.Asp90=
ENST00000638939.1:c.165C=	ENSP00000492052.1:p.Asp55=
ENST00000309641.10:c.408C=	ENSP00000308485.6:p.Asp136=
ENST00000340635.10:c.600C=	ENSP00000345502.6:p.Asp200=
ENST00000360047.9:c.192C=	ENSP00000353152.5:p.Asp64=
ENST00000405053.7:n.263C=
ENST00000405755.6:c.234C=	ENSP00000384806.2:p.Asp78=
ENST00000502484.6:c.417C=	ENSP00000423094.2:p.Asp139=
ENST00000502575.1:c.408C=	ENSP00000425917.1:p.Asp136=
ENST00000503258.5:c.210C=	ENSP00000425605.1:p.Asp70=
ENST00000505453.1:c.-98-176853C=	ENSP00000421013.1:n.-98-176853C=
ENST00000507116.5:c.408C=	ENSP00000424852.1:p.Asp136=
ENST00000514231.1:n.363C=
ENST00000515324.1:n.112C=
ENST00000546160.5:c.207C=	ENSP00000442734.2:p.Asp69=
ENST00000621323.4:n.145C=
NM_001104631.1:c.600C=	NP_001098101.1:p.Asp200=
NM_001165899.1:c.417C=	NP_001159371.1:p.Asp139=
NM_001197218.1:c.408C=	NP_001184147.1:p.Asp136=
NM_001197219.1:c.234C=	NP_001184148.1:p.Asp78=
NM_001197220.1:c.210C=	NP_001184149.1:p.Asp70=
NM_006203.4:c.192C=	NP_006194.2:p.Asp64=
XM_005248537.2:c.270C=	XP_005248594.1:p.Asp90=
XM_005248538.3:c.192C=	XP_005248595.1:p.Asp64=
XM_011543469.1:c.564C=	XP_011541771.1:p.Asp188=
XM_011543470.1:c.564C=	XP_011541772.1:p.Asp188=
XM_011543471.1:c.417C=	XP_011541773.1:p.Asp139=
XM_011543472.1:c.417C=	XP_011541774.1:p.Asp139=
XM_011543473.1:c.417C=	XP_011541775.1:p.Asp139=
XM_011543474.1:c.387C=	XP_011541776.1:p.Asp129=
XM_011543475.1:c.234C=	XP_011541777.1:p.Asp78=
XM_011543476.1:c.180C=	XP_011541778.1:p.Asp60=
XM_011543477.1:c.159C=	XP_011541779.1:p.Asp53=
XM_011543478.1:c.96C=	XP_011541780.1:p.Asp32=
XM_011543479.1:c.96C=	XP_011541781.1:p.Asp32=
NM_001349241.1:c.387C=	NP_001336170.1:p.Asp129=
NM_001349242.1:c.270C=	NP_001336171.1:p.Asp90=
NM_001349243.1:c.-95C=	NP_001336172.1:n.-95C=
NM_001364599.1:c.417C=	NP_001351528.1:p.Asp139=
NM_001364600.1:c.417C=	NP_001351529.1:p.Asp139=
NM_001364601.1:c.408C=	NP_001351530.1:p.Asp136=
NM_001364602.1:c.408C=	NP_001351531.1:p.Asp136=
NM_001364603.1:c.-351C=	NP_001351532.1:n.-351C=
NM_001364604.1:c.-95C=	NP_001351533.1:n.-95C=
XM_011543470.2:c.564C=	XP_011541772.1:p.Asp188=
XM_011543471.2:c.417C=	XP_011541773.1:p.Asp139=
XM_017009565.1:c.564C=	XP_016865054.1:p.Asp188=
XM_017009566.1:c.417C=	XP_016865055.1:p.Asp139=
XM_017009567.1:c.402C=	XP_016865056.1:p.Asp134=
XM_024446110.1:c.564C=	XP_024301878.1:p.Asp188=
XM_024446112.1:c.417C=	XP_024301880.1:p.Asp139=
NM_001104631.2:c.600C= MANE Select	NP_001098101.1:p.Asp200=
NM_001165899.2:c.417C=	NP_001159371.1:p.Asp139=
NM_001197218.2:c.408C=	NP_001184147.1:p.Asp136=
NM_001197219.2:c.234C=	NP_001184148.1:p.Asp78=
NM_001197220.2:c.210C=	NP_001184149.1:p.Asp70=
NM_001349241.2:c.387C=	NP_001336170.1:p.Asp129=
NM_001349243.2:c.-95C=	NP_001336172.1:n.-95C=
NM_001364600.2:c.417C=	NP_001351529.1:p.Asp139=
NM_001364602.2:c.408C=	NP_001351531.1:p.Asp136=
NM_001349242.2:c.270C=	NP_001336171.1:p.Asp90=
NM_006203.5:c.192C=	NP_006194.2:p.Asp64=