Canonical Allele Identifier: CA359930700
Gene: PDE4D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.59215795G>C , CM000667.2:g.59215795G>C GRCh38
NC_000005.9:g.58511621G>C , CM000667.1:g.58511621G>C GRCh37
NC_000005.8:g.58547378G>C NCBI36
NG_027957.1:g.1277305C>G
NG_027957.2:g.1313535C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000507116.6:c.437C>G ENSP00000424852.1:p.Ser146Cys
ENST00000340635.11:c.629C>G MANE Select ENSP00000345502.6:p.Ser210Cys
ENST00000636120.1:c.299C>G ENSP00000490821.1:p.Ser100Cys
ENST00000638939.1:c.194C>G ENSP00000492052.1:p.Ser65Cys
ENST00000309641.10:c.437C>G ENSP00000308485.6:p.Ser146Cys
ENST00000340635.10:c.629C>G ENSP00000345502.6:p.Ser210Cys
ENST00000360047.9:c.221C>G ENSP00000353152.5:p.Ser74Cys
ENST00000405053.7:n.292C>G
ENST00000405755.6:c.263C>G ENSP00000384806.2:p.Ser88Cys
ENST00000502484.6:c.446C>G ENSP00000423094.2:p.Ser149Cys
ENST00000502575.1:c.437C>G ENSP00000425917.1:p.Ser146Cys
ENST00000503258.5:c.239C>G ENSP00000425605.1:p.Ser80Cys
ENST00000505453.1:c.-98-176824C>G ENSP00000421013.1:n.-98-176824C>G
ENST00000507116.5:c.437C>G ENSP00000424852.1:p.Ser146Cys
ENST00000514231.1:n.392C>G
ENST00000515324.1:n.141C>G
ENST00000546160.5:c.236C>G ENSP00000442734.2:p.Ser79Cys
ENST00000621323.4:n.174C>G
NM_001104631.1:c.629C>G NP_001098101.1:p.Ser210Cys
NM_001165899.1:c.446C>G NP_001159371.1:p.Ser149Cys
NM_001197218.1:c.437C>G NP_001184147.1:p.Ser146Cys
NM_001197219.1:c.263C>G NP_001184148.1:p.Ser88Cys
NM_001197220.1:c.239C>G NP_001184149.1:p.Ser80Cys
NM_006203.4:c.221C>G NP_006194.2:p.Ser74Cys
XM_005248537.2:c.299C>G XP_005248594.1:p.Ser100Cys
XM_005248538.3:c.221C>G XP_005248595.1:p.Ser74Cys
XM_011543469.1:c.593C>G XP_011541771.1:p.Ser198Cys
XM_011543470.1:c.593C>G XP_011541772.1:p.Ser198Cys
XM_011543471.1:c.446C>G XP_011541773.1:p.Ser149Cys
XM_011543472.1:c.446C>G XP_011541774.1:p.Ser149Cys
XM_011543473.1:c.446C>G XP_011541775.1:p.Ser149Cys
XM_011543474.1:c.416C>G XP_011541776.1:p.Ser139Cys
XM_011543475.1:c.263C>G XP_011541777.1:p.Ser88Cys
XM_011543476.1:c.209C>G XP_011541778.1:p.Ser70Cys
XM_011543477.1:c.188C>G XP_011541779.1:p.Ser63Cys
XM_011543478.1:c.125C>G XP_011541780.1:p.Ser42Cys
XM_011543479.1:c.125C>G XP_011541781.1:p.Ser42Cys
NM_001349241.1:c.416C>G NP_001336170.1:p.Ser139Cys
NM_001349242.1:c.299C>G NP_001336171.1:p.Ser100Cys
NM_001349243.1:c.-66C>G NP_001336172.1:n.-66C>G
NM_001364599.1:c.446C>G NP_001351528.1:p.Ser149Cys
NM_001364600.1:c.446C>G NP_001351529.1:p.Ser149Cys
NM_001364601.1:c.437C>G NP_001351530.1:p.Ser146Cys
NM_001364602.1:c.437C>G NP_001351531.1:p.Ser146Cys
NM_001364603.1:c.-322C>G NP_001351532.1:n.-322C>G
NM_001364604.1:c.-66C>G NP_001351533.1:n.-66C>G
XM_011543470.2:c.593C>G XP_011541772.1:p.Ser198Cys
XM_011543471.2:c.446C>G XP_011541773.1:p.Ser149Cys
XM_017009565.1:c.593C>G XP_016865054.1:p.Ser198Cys
XM_017009566.1:c.446C>G XP_016865055.1:p.Ser149Cys
XM_017009567.1:c.431C>G XP_016865056.1:p.Ser144Cys
XM_024446110.1:c.593C>G XP_024301878.1:p.Ser198Cys
XM_024446112.1:c.446C>G XP_024301880.1:p.Ser149Cys
NM_001104631.2:c.629C>G MANE Select NP_001098101.1:p.Ser210Cys
NM_001165899.2:c.446C>G NP_001159371.1:p.Ser149Cys
NM_001197218.2:c.437C>G NP_001184147.1:p.Ser146Cys
NM_001197219.2:c.263C>G NP_001184148.1:p.Ser88Cys
NM_001197220.2:c.239C>G NP_001184149.1:p.Ser80Cys
NM_001349241.2:c.416C>G NP_001336170.1:p.Ser139Cys
NM_001349243.2:c.-66C>G NP_001336172.1:n.-66C>G
NM_001364600.2:c.446C>G NP_001351529.1:p.Ser149Cys
NM_001364602.2:c.437C>G NP_001351531.1:p.Ser146Cys
NM_001349242.2:c.299C>G NP_001336171.1:p.Ser100Cys
NM_006203.5:c.221C>G NP_006194.2:p.Ser74Cys