Canonical Allele Identifier: CA3276326

Gene: PDE4D

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.59180622G>T , CM000667.2:g.59180622G>T	GRCh38
NC_000005.9:g.58476448G>T , CM000667.1:g.58476448G>T	GRCh37
NC_000005.8:g.58512205G>T	NCBI36
NG_027957.1:g.1312478C>A
NG_027957.2:g.1348708C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001104631.2:c.781C>A MANE Select	NP_001098101.1:p.Pro261Thr
ENST00000340635.11:c.781C>A MANE Select	ENSP00000345502.6:p.Pro261Thr
NM_001104631.1:c.781C>A	NP_001098101.1:p.Pro261Thr
NM_001165899.1:c.598C>A	NP_001159371.1:p.Pro200Thr
NM_001165899.2:c.598C>A	NP_001159371.1:p.Pro200Thr
NM_001197218.1:c.589C>A	NP_001184147.1:p.Pro197Thr
NM_001197218.2:c.589C>A	NP_001184147.1:p.Pro197Thr
NM_001197219.1:c.415C>A	NP_001184148.1:p.Pro139Thr
NM_001197219.2:c.415C>A	NP_001184148.1:p.Pro139Thr
NM_001197220.1:c.391C>A	NP_001184149.1:p.Pro131Thr
NM_001197220.2:c.391C>A	NP_001184149.1:p.Pro131Thr
NM_001349241.1:c.568C>A	NP_001336170.1:p.Pro190Thr
NM_001349241.2:c.568C>A	NP_001336170.1:p.Pro190Thr
NM_001349242.1:c.451C>A	NP_001336171.1:p.Pro151Thr
NM_001349242.2:c.451C>A	NP_001336171.1:p.Pro151Thr
NM_001349243.1:c.13C>A	NP_001336172.1:p.Pro5Thr
NM_001349243.2:c.13C>A	NP_001336172.1:p.Pro5Thr
NM_001364599.1:c.598C>A	NP_001351528.1:p.Pro200Thr
NM_001364600.1:c.598C>A	NP_001351529.1:p.Pro200Thr
NM_001364600.2:c.598C>A	NP_001351529.1:p.Pro200Thr
NM_001364602.1:c.589C>A	NP_001351531.1:p.Pro197Thr
NM_001364602.2:c.589C>A	NP_001351531.1:p.Pro197Thr
NM_001364603.1:c.-170C>A	NP_001351532.1:n.-170C>A
NM_001364604.1:c.13C>A	NP_001351533.1:p.Pro5Thr
NM_006203.4:c.373C>A	NP_006194.2:p.Pro125Thr
NM_006203.5:c.373C>A	NP_006194.2:p.Pro125Thr
ENST00000309641.10:c.589C>A	ENSP00000308485.6:p.Pro197Thr
ENST00000340635.10:c.781C>A	ENSP00000345502.6:p.Pro261Thr
ENST00000360047.9:c.373C>A	ENSP00000353152.5:p.Pro125Thr
ENST00000405053.7:n.444C>A
ENST00000405755.6:c.415C>A	ENSP00000384806.2:p.Pro139Thr
ENST00000502484.6:c.598C>A	ENSP00000423094.2:p.Pro200Thr
ENST00000502575.1:c.589C>A	ENSP00000425917.1:p.Pro197Thr
ENST00000503258.5:c.391C>A	ENSP00000425605.1:p.Pro131Thr
ENST00000505453.1:c.-98-141651C>A	ENSP00000421013.1:n.-98-141651C>A
ENST00000507116.5:c.589C>A	ENSP00000424852.1:p.Pro197Thr
ENST00000507116.6:c.589C>A	ENSP00000424852.1:p.Pro197Thr
ENST00000515324.1:n.293C>A
ENST00000546160.5:c.388C>A	ENSP00000442734.2:p.Pro130Thr
ENST00000621323.4:n.326C>A
ENST00000636120.1:c.451C>A	ENSP00000490821.1:p.Pro151Thr
ENST00000638939.1:c.346C>A	ENSP00000492052.1:p.Pro116Thr
XM_005248537.2:c.451C>A	XP_005248594.1:p.Pro151Thr
XM_005248538.3:c.373C>A	XP_005248595.1:p.Pro125Thr
XM_011543469.1:c.745C>A	XP_011541771.1:p.Pro249Thr
XM_011543470.1:c.745C>A	XP_011541772.1:p.Pro249Thr
XM_011543470.2:c.745C>A	XP_011541772.1:p.Pro249Thr
XM_011543471.1:c.598C>A	XP_011541773.1:p.Pro200Thr
XM_011543471.2:c.598C>A	XP_011541773.1:p.Pro200Thr
XM_011543472.1:c.598C>A	XP_011541774.1:p.Pro200Thr
XM_011543473.1:c.598C>A	XP_011541775.1:p.Pro200Thr
XM_011543474.1:c.568C>A	XP_011541776.1:p.Pro190Thr
XM_011543475.1:c.415C>A	XP_011541777.1:p.Pro139Thr
XM_011543476.1:c.361C>A	XP_011541778.1:p.Pro121Thr
XM_011543477.1:c.340C>A	XP_011541779.1:p.Pro114Thr
XM_011543478.1:c.277C>A	XP_011541780.1:p.Pro93Thr
XM_011543479.1:c.277C>A	XP_011541781.1:p.Pro93Thr
XM_017009565.1:c.745C>A	XP_016865054.1:p.Pro249Thr
XM_017009566.1:c.598C>A	XP_016865055.1:p.Pro200Thr
XM_017009567.1:c.583C>A	XP_016865056.1:p.Pro195Thr
XM_024446110.1:c.745C>A	XP_024301878.1:p.Pro249Thr
XM_024446112.1:c.598C>A	XP_024301880.1:p.Pro200Thr