Canonical Allele Identifier: CA1549218568

Gene: PDE4D

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.59193522A= , CM000667.2:g.59193522A=	GRCh38
NC_000005.9:g.58489348A= , CM000667.1:g.58489348A=	GRCh37
NC_000005.8:g.58525105A=	NCBI36
NG_027957.1:g.1299578T=
NG_027957.2:g.1335808T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507116.6:c.470T=	ENSP00000424852.1:p.Leu157=
ENST00000340635.11:c.662T= MANE Select	ENSP00000345502.6:p.Leu221=
ENST00000636120.1:c.332T=	ENSP00000490821.1:p.Leu111=
ENST00000638939.1:c.227T=	ENSP00000492052.1:p.Leu76=
ENST00000309641.10:c.470T=	ENSP00000308485.6:p.Leu157=
ENST00000340635.10:c.662T=	ENSP00000345502.6:p.Leu221=
ENST00000360047.9:c.254T=	ENSP00000353152.5:p.Leu85=
ENST00000405053.7:n.325T=
ENST00000405755.6:c.296T=	ENSP00000384806.2:p.Leu99=
ENST00000502484.6:c.479T=	ENSP00000423094.2:p.Leu160=
ENST00000502575.1:c.470T=	ENSP00000425917.1:p.Leu157=
ENST00000503258.5:c.272T=	ENSP00000425605.1:p.Leu91=
ENST00000505453.1:c.-98-154551T=	ENSP00000421013.1:n.-98-154551T=
ENST00000507116.5:c.470T=	ENSP00000424852.1:p.Leu157=
ENST00000515324.1:n.174T=
ENST00000546160.5:c.269T=	ENSP00000442734.2:p.Leu90=
ENST00000621323.4:n.207T=
NM_001104631.1:c.662T=	NP_001098101.1:p.Leu221=
NM_001165899.1:c.479T=	NP_001159371.1:p.Leu160=
NM_001197218.1:c.470T=	NP_001184147.1:p.Leu157=
NM_001197219.1:c.296T=	NP_001184148.1:p.Leu99=
NM_001197220.1:c.272T=	NP_001184149.1:p.Leu91=
NM_006203.4:c.254T=	NP_006194.2:p.Leu85=
XM_005248537.2:c.332T=	XP_005248594.1:p.Leu111=
XM_005248538.3:c.254T=	XP_005248595.1:p.Leu85=
XM_011543469.1:c.626T=	XP_011541771.1:p.Leu209=
XM_011543470.1:c.626T=	XP_011541772.1:p.Leu209=
XM_011543471.1:c.479T=	XP_011541773.1:p.Leu160=
XM_011543472.1:c.479T=	XP_011541774.1:p.Leu160=
XM_011543473.1:c.479T=	XP_011541775.1:p.Leu160=
XM_011543474.1:c.449T=	XP_011541776.1:p.Leu150=
XM_011543475.1:c.296T=	XP_011541777.1:p.Leu99=
XM_011543476.1:c.242T=	XP_011541778.1:p.Leu81=
XM_011543477.1:c.221T=	XP_011541779.1:p.Leu74=
XM_011543478.1:c.158T=	XP_011541780.1:p.Leu53=
XM_011543479.1:c.158T=	XP_011541781.1:p.Leu53=
NM_001349241.1:c.449T=	NP_001336170.1:p.Leu150=
NM_001349242.1:c.332T=	NP_001336171.1:p.Leu111=
NM_001349243.1:c.-33T=	NP_001336172.1:n.-33T=
NM_001364599.1:c.479T=	NP_001351528.1:p.Leu160=
NM_001364600.1:c.479T=	NP_001351529.1:p.Leu160=
NM_001364602.1:c.470T=	NP_001351531.1:p.Leu157=
NM_001364603.1:c.-289T=	NP_001351532.1:n.-289T=
NM_001364604.1:c.-33T=	NP_001351533.1:n.-33T=
XM_011543470.2:c.626T=	XP_011541772.1:p.Leu209=
XM_011543471.2:c.479T=	XP_011541773.1:p.Leu160=
XM_017009565.1:c.626T=	XP_016865054.1:p.Leu209=
XM_017009566.1:c.479T=	XP_016865055.1:p.Leu160=
XM_017009567.1:c.464T=	XP_016865056.1:p.Leu155=
XM_024446110.1:c.626T=	XP_024301878.1:p.Leu209=
XM_024446112.1:c.479T=	XP_024301880.1:p.Leu160=
NM_001104631.2:c.662T= MANE Select	NP_001098101.1:p.Leu221=
NM_001165899.2:c.479T=	NP_001159371.1:p.Leu160=
NM_001197218.2:c.470T=	NP_001184147.1:p.Leu157=
NM_001197219.2:c.296T=	NP_001184148.1:p.Leu99=
NM_001197220.2:c.272T=	NP_001184149.1:p.Leu91=
NM_001349241.2:c.449T=	NP_001336170.1:p.Leu150=
NM_001349243.2:c.-33T=	NP_001336172.1:n.-33T=
NM_001364600.2:c.479T=	NP_001351529.1:p.Leu160=
NM_001364602.2:c.470T=	NP_001351531.1:p.Leu157=
NM_001349242.2:c.332T=	NP_001336171.1:p.Leu111=
NM_006203.5:c.254T=	NP_006194.2:p.Leu85=