Canonical Allele Identifier: CA359930603
Gene: PDE4D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.59215778T>C , CM000667.2:g.59215778T>C GRCh38
NC_000005.9:g.58511604T>C , CM000667.1:g.58511604T>C GRCh37
NC_000005.8:g.58547361T>C NCBI36
NG_027957.1:g.1277322A>G
NG_027957.2:g.1313552A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000507116.6:c.454A>G ENSP00000424852.1:p.Ile152Val
ENST00000340635.11:c.646A>G MANE Select ENSP00000345502.6:p.Ile216Val
ENST00000636120.1:c.316A>G ENSP00000490821.1:p.Ile106Val
ENST00000638939.1:c.211A>G ENSP00000492052.1:p.Ile71Val
ENST00000309641.10:c.454A>G ENSP00000308485.6:p.Ile152Val
ENST00000340635.10:c.646A>G ENSP00000345502.6:p.Ile216Val
ENST00000360047.9:c.238A>G ENSP00000353152.5:p.Ile80Val
ENST00000405053.7:n.309A>G
ENST00000405755.6:c.280A>G ENSP00000384806.2:p.Ile94Val
ENST00000502484.6:c.463A>G ENSP00000423094.2:p.Ile155Val
ENST00000502575.1:c.454A>G ENSP00000425917.1:p.Ile152Val
ENST00000503258.5:c.256A>G ENSP00000425605.1:p.Ile86Val
ENST00000505453.1:c.-98-176807A>G ENSP00000421013.1:n.-98-176807A>G
ENST00000507116.5:c.454A>G ENSP00000424852.1:p.Ile152Val
ENST00000514231.1:n.409A>G
ENST00000515324.1:n.158A>G
ENST00000546160.5:c.253A>G ENSP00000442734.2:p.Ile85Val
ENST00000621323.4:n.191A>G
NM_001104631.1:c.646A>G NP_001098101.1:p.Ile216Val
NM_001165899.1:c.463A>G NP_001159371.1:p.Ile155Val
NM_001197218.1:c.454A>G NP_001184147.1:p.Ile152Val
NM_001197219.1:c.280A>G NP_001184148.1:p.Ile94Val
NM_001197220.1:c.256A>G NP_001184149.1:p.Ile86Val
NM_006203.4:c.238A>G NP_006194.2:p.Ile80Val
XM_005248537.2:c.316A>G XP_005248594.1:p.Ile106Val
XM_005248538.3:c.238A>G XP_005248595.1:p.Ile80Val
XM_011543469.1:c.610A>G XP_011541771.1:p.Ile204Val
XM_011543470.1:c.610A>G XP_011541772.1:p.Ile204Val
XM_011543471.1:c.463A>G XP_011541773.1:p.Ile155Val
XM_011543472.1:c.463A>G XP_011541774.1:p.Ile155Val
XM_011543473.1:c.463A>G XP_011541775.1:p.Ile155Val
XM_011543474.1:c.433A>G XP_011541776.1:p.Ile145Val
XM_011543475.1:c.280A>G XP_011541777.1:p.Ile94Val
XM_011543476.1:c.226A>G XP_011541778.1:p.Ile76Val
XM_011543477.1:c.205A>G XP_011541779.1:p.Ile69Val
XM_011543478.1:c.142A>G XP_011541780.1:p.Ile48Val
XM_011543479.1:c.142A>G XP_011541781.1:p.Ile48Val
NM_001349241.1:c.433A>G NP_001336170.1:p.Ile145Val
NM_001349242.1:c.316A>G NP_001336171.1:p.Ile106Val
NM_001349243.1:c.-49A>G NP_001336172.1:n.-49A>G
NM_001364599.1:c.463A>G NP_001351528.1:p.Ile155Val
NM_001364600.1:c.463A>G NP_001351529.1:p.Ile155Val
NM_001364601.1:c.454A>G NP_001351530.1:p.Met152Val
NM_001364602.1:c.454A>G NP_001351531.1:p.Ile152Val
NM_001364603.1:c.-305A>G NP_001351532.1:n.-305A>G
NM_001364604.1:c.-49A>G NP_001351533.1:n.-49A>G
XM_011543470.2:c.610A>G XP_011541772.1:p.Ile204Val
XM_011543471.2:c.463A>G XP_011541773.1:p.Ile155Val
XM_017009565.1:c.610A>G XP_016865054.1:p.Ile204Val
XM_017009566.1:c.463A>G XP_016865055.1:p.Ile155Val
XM_017009567.1:c.448A>G XP_016865056.1:p.Ile150Val
XM_024446110.1:c.610A>G XP_024301878.1:p.Ile204Val
XM_024446112.1:c.463A>G XP_024301880.1:p.Ile155Val
NM_001104631.2:c.646A>G MANE Select NP_001098101.1:p.Ile216Val
NM_001165899.2:c.463A>G NP_001159371.1:p.Ile155Val
NM_001197218.2:c.454A>G NP_001184147.1:p.Ile152Val
NM_001197219.2:c.280A>G NP_001184148.1:p.Ile94Val
NM_001197220.2:c.256A>G NP_001184149.1:p.Ile86Val
NM_001349241.2:c.433A>G NP_001336170.1:p.Ile145Val
NM_001349243.2:c.-49A>G NP_001336172.1:n.-49A>G
NM_001364600.2:c.463A>G NP_001351529.1:p.Ile155Val
NM_001364602.2:c.454A>G NP_001351531.1:p.Ile152Val
NM_001349242.2:c.316A>G NP_001336171.1:p.Ile106Val
NM_006203.5:c.238A>G NP_006194.2:p.Ile80Val