Canonical Allele Identifier: CA1549218564

Gene: PDE4D

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.59193504G= , CM000667.2:g.59193504G=	GRCh38
NC_000005.9:g.58489330G= , CM000667.1:g.58489330G=	GRCh37
NC_000005.8:g.58525087G=	NCBI36
NG_027957.1:g.1299596C=
NG_027957.2:g.1335826C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507116.6:c.488C=	ENSP00000424852.1:p.Ala163=
ENST00000340635.11:c.680C= MANE Select	ENSP00000345502.6:p.Ala227=
ENST00000636120.1:c.350C=	ENSP00000490821.1:p.Ala117=
ENST00000638939.1:c.245C=	ENSP00000492052.1:p.Ala82=
ENST00000309641.10:c.488C=	ENSP00000308485.6:p.Ala163=
ENST00000340635.10:c.680C=	ENSP00000345502.6:p.Ala227=
ENST00000360047.9:c.272C=	ENSP00000353152.5:p.Ala91=
ENST00000405053.7:n.343C=
ENST00000405755.6:c.314C=	ENSP00000384806.2:p.Ala105=
ENST00000502484.6:c.497C=	ENSP00000423094.2:p.Ala166=
ENST00000502575.1:c.488C=	ENSP00000425917.1:p.Ala163=
ENST00000503258.5:c.290C=	ENSP00000425605.1:p.Ala97=
ENST00000505453.1:c.-98-154533C=	ENSP00000421013.1:n.-98-154533C=
ENST00000507116.5:c.488C=	ENSP00000424852.1:p.Ala163=
ENST00000515324.1:n.192C=
ENST00000546160.5:c.287C=	ENSP00000442734.2:p.Ala96=
ENST00000621323.4:n.225C=
NM_001104631.1:c.680C=	NP_001098101.1:p.Ala227=
NM_001165899.1:c.497C=	NP_001159371.1:p.Ala166=
NM_001197218.1:c.488C=	NP_001184147.1:p.Ala163=
NM_001197219.1:c.314C=	NP_001184148.1:p.Ala105=
NM_001197220.1:c.290C=	NP_001184149.1:p.Ala97=
NM_006203.4:c.272C=	NP_006194.2:p.Ala91=
XM_005248537.2:c.350C=	XP_005248594.1:p.Ala117=
XM_005248538.3:c.272C=	XP_005248595.1:p.Ala91=
XM_011543469.1:c.644C=	XP_011541771.1:p.Ala215=
XM_011543470.1:c.644C=	XP_011541772.1:p.Ala215=
XM_011543471.1:c.497C=	XP_011541773.1:p.Ala166=
XM_011543472.1:c.497C=	XP_011541774.1:p.Ala166=
XM_011543473.1:c.497C=	XP_011541775.1:p.Ala166=
XM_011543474.1:c.467C=	XP_011541776.1:p.Ala156=
XM_011543475.1:c.314C=	XP_011541777.1:p.Ala105=
XM_011543476.1:c.260C=	XP_011541778.1:p.Ala87=
XM_011543477.1:c.239C=	XP_011541779.1:p.Ala80=
XM_011543478.1:c.176C=	XP_011541780.1:p.Ala59=
XM_011543479.1:c.176C=	XP_011541781.1:p.Ala59=
NM_001349241.1:c.467C=	NP_001336170.1:p.Ala156=
NM_001349242.1:c.350C=	NP_001336171.1:p.Ala117=
NM_001349243.1:c.-15C=	NP_001336172.1:n.-15C=
NM_001364599.1:c.497C=	NP_001351528.1:p.Ala166=
NM_001364600.1:c.497C=	NP_001351529.1:p.Ala166=
NM_001364602.1:c.488C=	NP_001351531.1:p.Ala163=
NM_001364603.1:c.-271C=	NP_001351532.1:n.-271C=
NM_001364604.1:c.-15C=	NP_001351533.1:n.-15C=
XM_011543470.2:c.644C=	XP_011541772.1:p.Ala215=
XM_011543471.2:c.497C=	XP_011541773.1:p.Ala166=
XM_017009565.1:c.644C=	XP_016865054.1:p.Ala215=
XM_017009566.1:c.497C=	XP_016865055.1:p.Ala166=
XM_017009567.1:c.482C=	XP_016865056.1:p.Ala161=
XM_024446110.1:c.644C=	XP_024301878.1:p.Ala215=
XM_024446112.1:c.497C=	XP_024301880.1:p.Ala166=
NM_001104631.2:c.680C= MANE Select	NP_001098101.1:p.Ala227=
NM_001165899.2:c.497C=	NP_001159371.1:p.Ala166=
NM_001197218.2:c.488C=	NP_001184147.1:p.Ala163=
NM_001197219.2:c.314C=	NP_001184148.1:p.Ala105=
NM_001197220.2:c.290C=	NP_001184149.1:p.Ala97=
NM_001349241.2:c.467C=	NP_001336170.1:p.Ala156=
NM_001349243.2:c.-15C=	NP_001336172.1:n.-15C=
NM_001364600.2:c.497C=	NP_001351529.1:p.Ala166=
NM_001364602.2:c.488C=	NP_001351531.1:p.Ala163=
NM_001349242.2:c.350C=	NP_001336171.1:p.Ala117=
NM_006203.5:c.272C=	NP_006194.2:p.Ala91=