Canonical Allele Identifier: CA1549181867
Gene: PDE4D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.59111768C= , CM000667.2:g.59111768C= GRCh38
NC_000005.9:g.58407595C= , CM000667.1:g.58407595C= GRCh37
NC_000005.8:g.58443352C= NCBI36
NG_027957.1:g.1381331G=
NG_027957.2:g.1417562G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000507116.6:c.616+68827G= ENSP00000424852.1:n.616+68827G=
ENST00000340635.11:c.808+68827G= MANE Select ENSP00000345502.6:n.808+68827G=
ENST00000636120.1:c.478+68827G= ENSP00000490821.1:n.478+68827G=
ENST00000309641.10:c.617-20643G= ENSP00000308485.6:n.617-20643G=
ENST00000340635.10:c.808+68827G= ENSP00000345502.6:n.808+68827G=
ENST00000360047.9:c.400+68827G= ENSP00000353152.5:n.400+68827G=
ENST00000405053.7:n.471+68827G=
ENST00000405755.6:c.442+68827G= ENSP00000384806.2:n.442+68827G=
ENST00000502484.6:c.625+68827G= ENSP00000423094.2:n.625+68827G=
ENST00000503258.5:c.418+68827G= ENSP00000425605.1:n.418+68827G=
ENST00000505453.1:c.-98-72797G= ENSP00000421013.1:n.-98-72797G=
ENST00000507116.5:c.616+68827G= ENSP00000424852.1:n.616+68827G=
ENST00000546160.5:c.415+68827G= ENSP00000442734.2:n.415+68827G=
NM_001104631.1:c.808+68827G= NP_001098101.1:n.808+68827G=
NM_001165899.1:c.625+68827G= NP_001159371.1:n.625+68827G=
NM_001197218.1:c.616+68827G= NP_001184147.1:n.616+68827G=
NM_001197219.1:c.442+68827G= NP_001184148.1:n.442+68827G=
NM_001197220.1:c.418+68827G= NP_001184149.1:n.418+68827G=
NM_006203.4:c.400+68827G= NP_006194.2:n.400+68827G=
XM_005248537.2:c.478+68827G= XP_005248594.1:n.478+68827G=
XM_005248538.3:c.400+68827G= XP_005248595.1:n.400+68827G=
XM_011543469.1:c.772+68827G= XP_011541771.1:n.772+68827G=
XM_011543470.1:c.772+68827G= XP_011541772.1:n.772+68827G=
XM_011543471.1:c.625+68827G= XP_011541773.1:n.625+68827G=
XM_011543472.1:c.625+68827G= XP_011541774.1:n.625+68827G=
XM_011543473.1:c.625+68827G= XP_011541775.1:n.625+68827G=
XM_011543474.1:c.595+68827G= XP_011541776.1:n.595+68827G=
XM_011543475.1:c.442+68827G= XP_011541777.1:n.442+68827G=
XM_011543476.1:c.388+68827G= XP_011541778.1:n.388+68827G=
XM_011543477.1:c.367+68827G= XP_011541779.1:n.367+68827G=
XM_011543478.1:c.304+68827G= XP_011541780.1:n.304+68827G=
XM_011543479.1:c.304+68827G= XP_011541781.1:n.304+68827G=
NM_001349241.1:c.595+68827G= NP_001336170.1:n.595+68827G=
NM_001349242.1:c.478+68827G= NP_001336171.1:n.478+68827G=
NM_001349243.1:c.40+68827G= NP_001336172.1:n.40+68827G=
NM_001364599.1:c.625+68827G= NP_001351528.1:n.625+68827G=
NM_001364603.1:c.-142-20643G= NP_001351532.1:n.-142-20643G=
NM_001364604.1:c.40+68827G= NP_001351533.1:n.40+68827G=
XM_011543470.2:c.772+68827G= XP_011541772.1:n.772+68827G=
XM_011543471.2:c.625+68827G= XP_011541773.1:n.625+68827G=
XM_017009565.1:c.772+68827G= XP_016865054.1:n.772+68827G=
XM_017009566.1:c.625+68827G= XP_016865055.1:n.625+68827G=
XM_017009567.1:c.610+68827G= XP_016865056.1:n.610+68827G=
XM_024446110.1:c.772+68827G= XP_024301878.1:n.772+68827G=
XM_024446112.1:c.625+68827G= XP_024301880.1:n.625+68827G=
NM_001104631.2:c.808+68827G= MANE Select NP_001098101.1:n.808+68827G=
NM_001165899.2:c.625+68827G= NP_001159371.1:n.625+68827G=
NM_001197218.2:c.616+68827G= NP_001184147.1:n.616+68827G=
NM_001197219.2:c.442+68827G= NP_001184148.1:n.442+68827G=
NM_001197220.2:c.418+68827G= NP_001184149.1:n.418+68827G=
NM_001349241.2:c.595+68827G= NP_001336170.1:n.595+68827G=
NM_001349243.2:c.40+68827G= NP_001336172.1:n.40+68827G=
NM_001349242.2:c.478+68827G= NP_001336171.1:n.478+68827G=
NM_006203.5:c.400+68827G= NP_006194.2:n.400+68827G=