Canonical Allele Identifier: CA1549268809
Gene: PDE4D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.59303490C= , CM000667.2:g.59303490C= GRCh38
NC_000005.9:g.58599316C= , CM000667.1:g.58599316C= GRCh37
NC_000005.8:g.58635073C= NCBI36
NG_027957.1:g.1189610G=
NG_027957.2:g.1225840G=

Transcript Alleles

HGVS Amino-acid change
ENST00000507116.6:c.264-87522G= ENSP00000424852.1:n.264-87522G=
ENST00000340635.11:c.456-87522G= MANE Select ENSP00000345502.6:n.456-87522G=
ENST00000636120.1:c.126-87522G= ENSP00000490821.1:n.126-87522G=
ENST00000309641.10:c.264-87522G= ENSP00000308485.6:n.264-87522G=
ENST00000340635.10:c.456-87522G= ENSP00000345502.6:n.456-87522G=
ENST00000360047.9:c.48-87522G= ENSP00000353152.5:n.48-87522G=
ENST00000405053.7:n.119-87522G=
ENST00000405755.6:c.89+53268G= ENSP00000384806.2:n.89+53268G=
ENST00000502484.6:c.273-87522G= ENSP00000423094.2:n.273-87522G=
ENST00000502575.1:c.264-87522G= ENSP00000425917.1:n.264-87522G=
ENST00000505453.1:c.-98-264519G= ENSP00000421013.1:n.-98-264519G=
ENST00000507116.5:c.264-87522G= ENSP00000424852.1:n.264-87522G=
ENST00000514231.1:n.219-87522G=
NM_001104631.1:c.456-87522G= NP_001098101.1:n.456-87522G=
NM_001165899.1:c.273-87522G= NP_001159371.1:n.273-87522G=
NM_001197218.1:c.264-87522G= NP_001184147.1:n.264-87522G=
NM_001197219.1:c.89+53268G= NP_001184148.1:n.89+53268G=
NM_006203.4:c.48-87522G= NP_006194.2:n.48-87522G=
XM_005248537.2:c.126-87522G= XP_005248594.1:n.126-87522G=
XM_005248538.3:c.48-87522G= XP_005248595.1:n.48-87522G=
XM_011543469.1:c.420-87522G= XP_011541771.1:n.420-87522G=
XM_011543470.1:c.420-87522G= XP_011541772.1:n.420-87522G=
XM_011543471.1:c.273-87522G= XP_011541773.1:n.273-87522G=
XM_011543472.1:c.273-87522G= XP_011541774.1:n.273-87522G=
XM_011543473.1:c.273-87522G= XP_011541775.1:n.273-87522G=
XM_011543474.1:c.243-87522G= XP_011541776.1:n.243-87522G=
XM_011543475.1:c.90-87522G= XP_011541777.1:n.90-87522G=
XM_011543476.1:c.36-87522G= XP_011541778.1:n.36-87522G=
XM_011543477.1:c.15-87522G= XP_011541779.1:n.15-87522G=
XM_011543478.1:c.-50+79280G= XP_011541780.1:n.-50+79280G=
NM_001349241.1:c.243-87522G= NP_001336170.1:n.243-87522G=
NM_001349242.1:c.126-87522G= NP_001336171.1:n.126-87522G=
NM_001349243.1:c.-239-87522G= NP_001336172.1:n.-239-87522G=
NM_001364599.1:c.273-87522G= NP_001351528.1:n.273-87522G=
NM_001364600.1:c.273-87522G= NP_001351529.1:n.273-87522G=
NM_001364601.1:c.264-87522G= NP_001351530.1:n.264-87522G=
NM_001364602.1:c.264-87522G= NP_001351531.1:n.264-87522G=
NM_001364603.1:c.-495-87522G= NP_001351532.1:n.-495-87522G=
NM_001364604.1:c.-239-87522G= NP_001351533.1:n.-239-87522G=
XM_011543470.2:c.420-87522G= XP_011541772.1:n.420-87522G=
XM_011543471.2:c.273-87522G= XP_011541773.1:n.273-87522G=
XM_017009565.1:c.420-87522G= XP_016865054.1:n.420-87522G=
XM_017009566.1:c.273-87522G= XP_016865055.1:n.273-87522G=
XM_017009567.1:c.258-87522G= XP_016865056.1:n.258-87522G=
XM_024446110.1:c.420-87522G= XP_024301878.1:n.420-87522G=
XM_024446112.1:c.273-87522G= XP_024301880.1:n.273-87522G=
NM_001104631.2:c.456-87522G= MANE Select NP_001098101.1:n.456-87522G=
NM_001165899.2:c.273-87522G= NP_001159371.1:n.273-87522G=
NM_001197218.2:c.264-87522G= NP_001184147.1:n.264-87522G=
NM_001197219.2:c.89+53268G= NP_001184148.1:n.89+53268G=
NM_001349241.2:c.243-87522G= NP_001336170.1:n.243-87522G=
NM_001349243.2:c.-239-87522G= NP_001336172.1:n.-239-87522G=
NM_001364600.2:c.273-87522G= NP_001351529.1:n.273-87522G=
NM_001364602.2:c.264-87522G= NP_001351531.1:n.264-87522G=
NM_001349242.2:c.126-87522G= NP_001336171.1:n.126-87522G=
NM_006203.5:c.48-87522G= NP_006194.2:n.48-87522G=