Canonical Allele Identifier: CA1549150257
Gene: PDE4D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.59038899A= , CM000667.2:g.59038899A= GRCh38
NC_000005.9:g.58334726A= , CM000667.1:g.58334726A= GRCh37
NC_000005.8:g.58370483A= NCBI36
NG_027957.1:g.1454200T=
NG_027957.2:g.1490431T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000507116.6:c.689T= ENSP00000424852.1:p.Leu230=
ENST00000340635.11:c.881T= MANE Select ENSP00000345502.6:p.Leu294=
ENST00000636120.1:c.551T= ENSP00000490821.1:p.Leu184=
ENST00000309641.10:c.733T= ENSP00000308485.6:n.733T=
ENST00000340635.10:c.881T= ENSP00000345502.6:p.Leu294=
ENST00000358923.10:c.-26T= ENSP00000351800.6:n.-26T=
ENST00000360047.9:c.473T= ENSP00000353152.5:p.Leu158=
ENST00000405053.7:n.472-45434T=
ENST00000405755.6:c.515T= ENSP00000384806.2:p.Leu172=
ENST00000502484.6:c.698T= ENSP00000423094.2:p.Leu233=
ENST00000503258.5:c.491T= ENSP00000425605.1:p.Leu164=
ENST00000505453.1:c.-26T= ENSP00000421013.1:n.-26T=
ENST00000507116.5:c.689T= ENSP00000424852.1:p.Leu230=
ENST00000515011.5:n.617T=
ENST00000546160.5:c.488T= ENSP00000442734.2:p.Leu163=
NM_001104631.1:c.881T= NP_001098101.1:p.Leu294=
NM_001165899.1:c.698T= NP_001159371.1:p.Leu233=
NM_001197218.1:c.689T= NP_001184147.1:p.Leu230=
NM_001197219.1:c.515T= NP_001184148.1:p.Leu172=
NM_001197220.1:c.491T= NP_001184149.1:p.Leu164=
NM_001197221.1:c.-26T= NP_001184150.1:n.-26T=
NM_001197222.1:c.209T= NP_001184151.1:p.Leu70=
NM_006203.4:c.473T= NP_006194.2:p.Leu158=
XM_005248537.2:c.551T= XP_005248594.1:p.Leu184=
XM_005248538.3:c.473T= XP_005248595.1:p.Leu158=
XM_011543469.1:c.845T= XP_011541771.1:p.Leu282=
XM_011543470.1:c.845T= XP_011541772.1:p.Leu282=
XM_011543471.1:c.698T= XP_011541773.1:p.Leu233=
XM_011543472.1:c.698T= XP_011541774.1:p.Leu233=
XM_011543473.1:c.698T= XP_011541775.1:p.Leu233=
XM_011543474.1:c.668T= XP_011541776.1:p.Leu223=
XM_011543475.1:c.515T= XP_011541777.1:p.Leu172=
XM_011543476.1:c.461T= XP_011541778.1:p.Leu154=
XM_011543477.1:c.440T= XP_011541779.1:p.Leu147=
XM_011543478.1:c.377T= XP_011541780.1:p.Leu126=
XM_011543479.1:c.377T= XP_011541781.1:p.Leu126=
XR_948360.1:n.838+3781A=
NM_001349241.1:c.668T= NP_001336170.1:p.Leu223=
NM_001349242.1:c.551T= NP_001336171.1:p.Leu184=
NM_001349243.1:c.113T= NP_001336172.1:p.Leu38=
NM_001364599.1:c.698T= NP_001351528.1:p.Leu233=
NM_001364603.1:c.-26T= NP_001351532.1:n.-26T=
NM_001364604.1:c.113T= NP_001351533.1:p.Leu38=
XM_011543470.2:c.845T= XP_011541772.1:p.Leu282=
XM_011543471.2:c.698T= XP_011541773.1:p.Leu233=
XM_017009565.1:c.845T= XP_016865054.1:p.Leu282=
XM_017009566.1:c.698T= XP_016865055.1:p.Leu233=
XM_017009567.1:c.683T= XP_016865056.1:p.Leu228=
XM_024446110.1:c.845T= XP_024301878.1:p.Leu282=
XM_024446112.1:c.698T= XP_024301880.1:p.Leu233=
NM_001104631.2:c.881T= MANE Select NP_001098101.1:p.Leu294=
NM_001165899.2:c.698T= NP_001159371.1:p.Leu233=
NM_001197218.2:c.689T= NP_001184147.1:p.Leu230=
NM_001197219.2:c.515T= NP_001184148.1:p.Leu172=
NM_001197220.2:c.491T= NP_001184149.1:p.Leu164=
NM_001197221.2:c.-26T= NP_001184150.1:n.-26T=
NM_001197222.2:c.209T= NP_001184151.1:p.Leu70=
NM_001349241.2:c.668T= NP_001336170.1:p.Leu223=
NM_001349243.2:c.113T= NP_001336172.1:p.Leu38=
NM_001349242.2:c.551T= NP_001336171.1:p.Leu184=
NM_006203.5:c.473T= NP_006194.2:p.Leu158=