Canonical Allele Identifier: CA359930777
Gene: PDE4D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.59215812C>G , CM000667.2:g.59215812C>G GRCh38
NC_000005.9:g.58511638C>G , CM000667.1:g.58511638C>G GRCh37
NC_000005.8:g.58547395C>G NCBI36
NG_027957.1:g.1277288G>C
NG_027957.2:g.1313518G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000507116.6:c.420G>C ENSP00000424852.1:p.Lys140Asn
ENST00000340635.11:c.612G>C MANE Select ENSP00000345502.6:p.Lys204Asn
ENST00000636120.1:c.282G>C ENSP00000490821.1:p.Lys94Asn
ENST00000638939.1:c.177G>C ENSP00000492052.1:p.Lys59Asn
ENST00000309641.10:c.420G>C ENSP00000308485.6:p.Lys140Asn
ENST00000340635.10:c.612G>C ENSP00000345502.6:p.Lys204Asn
ENST00000360047.9:c.204G>C ENSP00000353152.5:p.Lys68Asn
ENST00000405053.7:n.275G>C
ENST00000405755.6:c.246G>C ENSP00000384806.2:p.Lys82Asn
ENST00000502484.6:c.429G>C ENSP00000423094.2:p.Lys143Asn
ENST00000502575.1:c.420G>C ENSP00000425917.1:p.Lys140Asn
ENST00000503258.5:c.222G>C ENSP00000425605.1:p.Lys74Asn
ENST00000505453.1:c.-98-176841G>C ENSP00000421013.1:n.-98-176841G>C
ENST00000507116.5:c.420G>C ENSP00000424852.1:p.Lys140Asn
ENST00000514231.1:n.375G>C
ENST00000515324.1:n.124G>C
ENST00000546160.5:c.219G>C ENSP00000442734.2:p.Lys73Asn
ENST00000621323.4:n.157G>C
NM_001104631.1:c.612G>C NP_001098101.1:p.Lys204Asn
NM_001165899.1:c.429G>C NP_001159371.1:p.Lys143Asn
NM_001197218.1:c.420G>C NP_001184147.1:p.Lys140Asn
NM_001197219.1:c.246G>C NP_001184148.1:p.Lys82Asn
NM_001197220.1:c.222G>C NP_001184149.1:p.Lys74Asn
NM_006203.4:c.204G>C NP_006194.2:p.Lys68Asn
XM_005248537.2:c.282G>C XP_005248594.1:p.Lys94Asn
XM_005248538.3:c.204G>C XP_005248595.1:p.Lys68Asn
XM_011543469.1:c.576G>C XP_011541771.1:p.Lys192Asn
XM_011543470.1:c.576G>C XP_011541772.1:p.Lys192Asn
XM_011543471.1:c.429G>C XP_011541773.1:p.Lys143Asn
XM_011543472.1:c.429G>C XP_011541774.1:p.Lys143Asn
XM_011543473.1:c.429G>C XP_011541775.1:p.Lys143Asn
XM_011543474.1:c.399G>C XP_011541776.1:p.Lys133Asn
XM_011543475.1:c.246G>C XP_011541777.1:p.Lys82Asn
XM_011543476.1:c.192G>C XP_011541778.1:p.Lys64Asn
XM_011543477.1:c.171G>C XP_011541779.1:p.Lys57Asn
XM_011543478.1:c.108G>C XP_011541780.1:p.Lys36Asn
XM_011543479.1:c.108G>C XP_011541781.1:p.Lys36Asn
NM_001349241.1:c.399G>C NP_001336170.1:p.Lys133Asn
NM_001349242.1:c.282G>C NP_001336171.1:p.Lys94Asn
NM_001349243.1:c.-83G>C NP_001336172.1:n.-83G>C
NM_001364599.1:c.429G>C NP_001351528.1:p.Lys143Asn
NM_001364600.1:c.429G>C NP_001351529.1:p.Lys143Asn
NM_001364601.1:c.420G>C NP_001351530.1:p.Lys140Asn
NM_001364602.1:c.420G>C NP_001351531.1:p.Lys140Asn
NM_001364603.1:c.-339G>C NP_001351532.1:n.-339G>C
NM_001364604.1:c.-83G>C NP_001351533.1:n.-83G>C
XM_011543470.2:c.576G>C XP_011541772.1:p.Lys192Asn
XM_011543471.2:c.429G>C XP_011541773.1:p.Lys143Asn
XM_017009565.1:c.576G>C XP_016865054.1:p.Lys192Asn
XM_017009566.1:c.429G>C XP_016865055.1:p.Lys143Asn
XM_017009567.1:c.414G>C XP_016865056.1:p.Lys138Asn
XM_024446110.1:c.576G>C XP_024301878.1:p.Lys192Asn
XM_024446112.1:c.429G>C XP_024301880.1:p.Lys143Asn
NM_001104631.2:c.612G>C MANE Select NP_001098101.1:p.Lys204Asn
NM_001165899.2:c.429G>C NP_001159371.1:p.Lys143Asn
NM_001197218.2:c.420G>C NP_001184147.1:p.Lys140Asn
NM_001197219.2:c.246G>C NP_001184148.1:p.Lys82Asn
NM_001197220.2:c.222G>C NP_001184149.1:p.Lys74Asn
NM_001349241.2:c.399G>C NP_001336170.1:p.Lys133Asn
NM_001349243.2:c.-83G>C NP_001336172.1:n.-83G>C
NM_001364600.2:c.429G>C NP_001351529.1:p.Lys143Asn
NM_001364602.2:c.420G>C NP_001351531.1:p.Lys140Asn
NM_001349242.2:c.282G>C NP_001336171.1:p.Lys94Asn
NM_006203.5:c.204G>C NP_006194.2:p.Lys68Asn