Canonical Allele Identifier: CA1549229305
Gene: PDE4D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.59215777A= , CM000667.2:g.59215777A= GRCh38
NC_000005.9:g.58511603A= , CM000667.1:g.58511603A= GRCh37
NC_000005.8:g.58547360A= NCBI36
NG_027957.1:g.1277323T=
NG_027957.2:g.1313553T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000507116.6:c.455T= ENSP00000424852.1:p.Ile152=
ENST00000340635.11:c.647T= MANE Select ENSP00000345502.6:p.Ile216=
ENST00000636120.1:c.317T= ENSP00000490821.1:p.Ile106=
ENST00000638939.1:c.212T= ENSP00000492052.1:p.Ile71=
ENST00000309641.10:c.455T= ENSP00000308485.6:p.Ile152=
ENST00000340635.10:c.647T= ENSP00000345502.6:p.Ile216=
ENST00000360047.9:c.239T= ENSP00000353152.5:p.Ile80=
ENST00000405053.7:n.310T=
ENST00000405755.6:c.281T= ENSP00000384806.2:p.Ile94=
ENST00000502484.6:c.464T= ENSP00000423094.2:p.Ile155=
ENST00000502575.1:c.455T= ENSP00000425917.1:p.Ile152=
ENST00000503258.5:c.257T= ENSP00000425605.1:p.Ile86=
ENST00000505453.1:c.-98-176806T= ENSP00000421013.1:n.-98-176806T=
ENST00000507116.5:c.455T= ENSP00000424852.1:p.Ile152=
ENST00000514231.1:n.410T=
ENST00000515324.1:n.159T=
ENST00000546160.5:c.254T= ENSP00000442734.2:p.Ile85=
ENST00000621323.4:n.192T=
NM_001104631.1:c.647T= NP_001098101.1:p.Ile216=
NM_001165899.1:c.464T= NP_001159371.1:p.Ile155=
NM_001197218.1:c.455T= NP_001184147.1:p.Ile152=
NM_001197219.1:c.281T= NP_001184148.1:p.Ile94=
NM_001197220.1:c.257T= NP_001184149.1:p.Ile86=
NM_006203.4:c.239T= NP_006194.2:p.Ile80=
XM_005248537.2:c.317T= XP_005248594.1:p.Ile106=
XM_005248538.3:c.239T= XP_005248595.1:p.Ile80=
XM_011543469.1:c.611T= XP_011541771.1:p.Ile204=
XM_011543470.1:c.611T= XP_011541772.1:p.Ile204=
XM_011543471.1:c.464T= XP_011541773.1:p.Ile155=
XM_011543472.1:c.464T= XP_011541774.1:p.Ile155=
XM_011543473.1:c.464T= XP_011541775.1:p.Ile155=
XM_011543474.1:c.434T= XP_011541776.1:p.Ile145=
XM_011543475.1:c.281T= XP_011541777.1:p.Ile94=
XM_011543476.1:c.227T= XP_011541778.1:p.Ile76=
XM_011543477.1:c.206T= XP_011541779.1:p.Ile69=
XM_011543478.1:c.143T= XP_011541780.1:p.Ile48=
XM_011543479.1:c.143T= XP_011541781.1:p.Ile48=
NM_001349241.1:c.434T= NP_001336170.1:p.Ile145=
NM_001349242.1:c.317T= NP_001336171.1:p.Ile106=
NM_001349243.1:c.-48T= NP_001336172.1:n.-48T=
NM_001364599.1:c.464T= NP_001351528.1:p.Ile155=
NM_001364600.1:c.464T= NP_001351529.1:p.Ile155=
NM_001364601.1:c.455T= NP_001351530.1:p.Met152=
NM_001364602.1:c.455T= NP_001351531.1:p.Ile152=
NM_001364603.1:c.-304T= NP_001351532.1:n.-304T=
NM_001364604.1:c.-48T= NP_001351533.1:n.-48T=
XM_011543470.2:c.611T= XP_011541772.1:p.Ile204=
XM_011543471.2:c.464T= XP_011541773.1:p.Ile155=
XM_017009565.1:c.611T= XP_016865054.1:p.Ile204=
XM_017009566.1:c.464T= XP_016865055.1:p.Ile155=
XM_017009567.1:c.449T= XP_016865056.1:p.Ile150=
XM_024446110.1:c.611T= XP_024301878.1:p.Ile204=
XM_024446112.1:c.464T= XP_024301880.1:p.Ile155=
NM_001104631.2:c.647T= MANE Select NP_001098101.1:p.Ile216=
NM_001165899.2:c.464T= NP_001159371.1:p.Ile155=
NM_001197218.2:c.455T= NP_001184147.1:p.Ile152=
NM_001197219.2:c.281T= NP_001184148.1:p.Ile94=
NM_001197220.2:c.257T= NP_001184149.1:p.Ile86=
NM_001349241.2:c.434T= NP_001336170.1:p.Ile145=
NM_001349243.2:c.-48T= NP_001336172.1:n.-48T=
NM_001364600.2:c.464T= NP_001351529.1:p.Ile155=
NM_001364602.2:c.455T= NP_001351531.1:p.Ile152=
NM_001349242.2:c.317T= NP_001336171.1:p.Ile106=
NM_006203.5:c.239T= NP_006194.2:p.Ile80=