Canonical Allele Identifier: CA359930866
Gene: PDE4D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.59215844G>C , CM000667.2:g.59215844G>C GRCh38
NC_000005.9:g.58511670G>C , CM000667.1:g.58511670G>C GRCh37
NC_000005.8:g.58547427G>C NCBI36
NG_027957.1:g.1277256C>G
NG_027957.2:g.1313486C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000507116.6:c.388C>G ENSP00000424852.1:p.Arg130Gly
ENST00000340635.11:c.580C>G MANE Select ENSP00000345502.6:p.Arg194Gly
ENST00000636120.1:c.250C>G ENSP00000490821.1:p.Arg84Gly
ENST00000638939.1:c.145C>G ENSP00000492052.1:p.Arg49Gly
ENST00000309641.10:c.388C>G ENSP00000308485.6:p.Arg130Gly
ENST00000340635.10:c.580C>G ENSP00000345502.6:p.Arg194Gly
ENST00000360047.9:c.172C>G ENSP00000353152.5:p.Arg58Gly
ENST00000405053.7:n.243C>G
ENST00000405755.6:c.214C>G ENSP00000384806.2:p.Arg72Gly
ENST00000502484.6:c.397C>G ENSP00000423094.2:p.Arg133Gly
ENST00000502575.1:c.388C>G ENSP00000425917.1:p.Arg130Gly
ENST00000503258.5:c.190C>G ENSP00000425605.1:p.Arg64Gly
ENST00000505453.1:c.-98-176873C>G ENSP00000421013.1:n.-98-176873C>G
ENST00000507116.5:c.388C>G ENSP00000424852.1:p.Arg130Gly
ENST00000514231.1:n.343C>G
ENST00000515324.1:n.92C>G
ENST00000546160.5:c.187C>G ENSP00000442734.2:p.Arg63Gly
ENST00000621323.4:n.125C>G
NM_001104631.1:c.580C>G NP_001098101.1:p.Arg194Gly
NM_001165899.1:c.397C>G NP_001159371.1:p.Arg133Gly
NM_001197218.1:c.388C>G NP_001184147.1:p.Arg130Gly
NM_001197219.1:c.214C>G NP_001184148.1:p.Arg72Gly
NM_001197220.1:c.190C>G NP_001184149.1:p.Arg64Gly
NM_006203.4:c.172C>G NP_006194.2:p.Arg58Gly
XM_005248537.2:c.250C>G XP_005248594.1:p.Arg84Gly
XM_005248538.3:c.172C>G XP_005248595.1:p.Arg58Gly
XM_011543469.1:c.544C>G XP_011541771.1:p.Arg182Gly
XM_011543470.1:c.544C>G XP_011541772.1:p.Arg182Gly
XM_011543471.1:c.397C>G XP_011541773.1:p.Arg133Gly
XM_011543472.1:c.397C>G XP_011541774.1:p.Arg133Gly
XM_011543473.1:c.397C>G XP_011541775.1:p.Arg133Gly
XM_011543474.1:c.367C>G XP_011541776.1:p.Arg123Gly
XM_011543475.1:c.214C>G XP_011541777.1:p.Arg72Gly
XM_011543476.1:c.160C>G XP_011541778.1:p.Arg54Gly
XM_011543477.1:c.139C>G XP_011541779.1:p.Arg47Gly
XM_011543478.1:c.76C>G XP_011541780.1:p.Arg26Gly
XM_011543479.1:c.76C>G XP_011541781.1:p.Arg26Gly
NM_001349241.1:c.367C>G NP_001336170.1:p.Arg123Gly
NM_001349242.1:c.250C>G NP_001336171.1:p.Arg84Gly
NM_001349243.1:c.-115C>G NP_001336172.1:n.-115C>G
NM_001364599.1:c.397C>G NP_001351528.1:p.Arg133Gly
NM_001364600.1:c.397C>G NP_001351529.1:p.Arg133Gly
NM_001364601.1:c.388C>G NP_001351530.1:p.Arg130Gly
NM_001364602.1:c.388C>G NP_001351531.1:p.Arg130Gly
NM_001364603.1:c.-371C>G NP_001351532.1:n.-371C>G
NM_001364604.1:c.-115C>G NP_001351533.1:n.-115C>G
XM_011543470.2:c.544C>G XP_011541772.1:p.Arg182Gly
XM_011543471.2:c.397C>G XP_011541773.1:p.Arg133Gly
XM_017009565.1:c.544C>G XP_016865054.1:p.Arg182Gly
XM_017009566.1:c.397C>G XP_016865055.1:p.Arg133Gly
XM_017009567.1:c.382C>G XP_016865056.1:p.Arg128Gly
XM_024446110.1:c.544C>G XP_024301878.1:p.Arg182Gly
XM_024446112.1:c.397C>G XP_024301880.1:p.Arg133Gly
NM_001104631.2:c.580C>G MANE Select NP_001098101.1:p.Arg194Gly
NM_001165899.2:c.397C>G NP_001159371.1:p.Arg133Gly
NM_001197218.2:c.388C>G NP_001184147.1:p.Arg130Gly
NM_001197219.2:c.214C>G NP_001184148.1:p.Arg72Gly
NM_001197220.2:c.190C>G NP_001184149.1:p.Arg64Gly
NM_001349241.2:c.367C>G NP_001336170.1:p.Arg123Gly
NM_001349243.2:c.-115C>G NP_001336172.1:n.-115C>G
NM_001364600.2:c.397C>G NP_001351529.1:p.Arg133Gly
NM_001364602.2:c.388C>G NP_001351531.1:p.Arg130Gly
NM_001349242.2:c.250C>G NP_001336171.1:p.Arg84Gly
NM_006203.5:c.172C>G NP_006194.2:p.Arg58Gly