Canonical Allele Identifier: CA1549304365

Gene: PDE4D

Linked Data

• dbSNP Id: rs181736

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.59381407G>C , CM000667.2:g.59381407G>C	GRCh38
NC_000005.9:g.58677233G>C , CM000667.1:g.58677233G>C	GRCh37
NC_000005.8:g.58712990G>C	NCBI36
NG_027957.1:g.1111693C>G
NG_027957.2:g.1147923C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000507116.6:c.264-165439C>G	ENSP00000424852.1:n.264-165439C>G
ENST00000340635.11:c.456-165439C>G MANE Select	ENSP00000345502.6:n.456-165439C>G
ENST00000636120.1:c.125+48887C>G	ENSP00000490821.1:n.125+48887C>G
ENST00000309641.10:c.264-165439C>G	ENSP00000308485.6:n.264-165439C>G
ENST00000340635.10:c.456-165439C>G	ENSP00000345502.6:n.456-165439C>G
ENST00000360047.9:c.48-165439C>G	ENSP00000353152.5:n.48-165439C>G
ENST00000405053.7:n.119-165439C>G
ENST00000502484.6:c.273-165439C>G	ENSP00000423094.2:n.273-165439C>G
ENST00000502575.1:c.264-165439C>G	ENSP00000425917.1:n.264-165439C>G
ENST00000505453.1:c.-99+204922C>G	ENSP00000421013.1:n.-99+204922C>G
ENST00000507116.5:c.264-165439C>G	ENSP00000424852.1:n.264-165439C>G
ENST00000514231.1:n.219-165439C>G
NM_001104631.1:c.456-165439C>G	NP_001098101.1:n.456-165439C>G
NM_001165899.1:c.273-165439C>G	NP_001159371.1:n.273-165439C>G
NM_001197218.1:c.264-165439C>G	NP_001184147.1:n.264-165439C>G
NM_006203.4:c.48-165439C>G	NP_006194.2:n.48-165439C>G
XM_005248537.2:c.125+48887C>G	XP_005248594.1:n.125+48887C>G
XM_005248538.3:c.48-165439C>G	XP_005248595.1:n.48-165439C>G
XM_011543469.1:c.420-165439C>G	XP_011541771.1:n.420-165439C>G
XM_011543470.1:c.420-165439C>G	XP_011541772.1:n.420-165439C>G
XM_011543471.1:c.273-165439C>G	XP_011541773.1:n.273-165439C>G
XM_011543472.1:c.273-165439C>G	XP_011541774.1:n.273-165439C>G
XM_011543473.1:c.273-165439C>G	XP_011541775.1:n.273-165439C>G
XM_011543474.1:c.243-165439C>G	XP_011541776.1:n.243-165439C>G
XM_011543475.1:c.89+148920C>G	XP_011541777.1:n.89+148920C>G
XM_011543476.1:c.35+53035C>G	XP_011541778.1:n.35+53035C>G
XM_011543477.1:c.15-165439C>G	XP_011541779.1:n.15-165439C>G
XM_011543478.1:c.-50+1363C>G	XP_011541780.1:n.-50+1363C>G
NM_001349241.1:c.243-165439C>G	NP_001336170.1:n.243-165439C>G
NM_001349242.1:c.125+48887C>G	NP_001336171.1:n.125+48887C>G
NM_001349243.1:c.-239-165439C>G	NP_001336172.1:n.-239-165439C>G
NM_001364599.1:c.273-165439C>G	NP_001351528.1:n.273-165439C>G
NM_001364600.1:c.273-165439C>G	NP_001351529.1:n.273-165439C>G
NM_001364601.1:c.264-165439C>G	NP_001351530.1:n.264-165439C>G
NM_001364602.1:c.264-165439C>G	NP_001351531.1:n.264-165439C>G
NM_001364603.1:c.-495-165439C>G	NP_001351532.1:n.-495-165439C>G
NM_001364604.1:c.-239-165439C>G	NP_001351533.1:n.-239-165439C>G
XM_011543470.2:c.420-165439C>G	XP_011541772.1:n.420-165439C>G
XM_011543471.2:c.273-165439C>G	XP_011541773.1:n.273-165439C>G
XM_017009565.1:c.420-165439C>G	XP_016865054.1:n.420-165439C>G
XM_017009566.1:c.273-165439C>G	XP_016865055.1:n.273-165439C>G
XM_017009567.1:c.258-165439C>G	XP_016865056.1:n.258-165439C>G
XM_024446110.1:c.420-165439C>G	XP_024301878.1:n.420-165439C>G
XM_024446112.1:c.273-165439C>G	XP_024301880.1:n.273-165439C>G
XR_001742411.1:n.3057C>G
NM_001104631.2:c.456-165439C>G MANE Select	NP_001098101.1:n.456-165439C>G
NM_001165899.2:c.273-165439C>G	NP_001159371.1:n.273-165439C>G
NM_001197218.2:c.264-165439C>G	NP_001184147.1:n.264-165439C>G
NM_001349241.2:c.243-165439C>G	NP_001336170.1:n.243-165439C>G
NM_001349243.2:c.-239-165439C>G	NP_001336172.1:n.-239-165439C>G
NM_001364600.2:c.273-165439C>G	NP_001351529.1:n.273-165439C>G
NM_001364602.2:c.264-165439C>G	NP_001351531.1:n.264-165439C>G
NM_001349242.2:c.125+48887C>G	NP_001336171.1:n.125+48887C>G
NM_006203.5:c.48-165439C>G	NP_006194.2:n.48-165439C>G