Canonical Allele Identifier: CA1549380881

Gene: PDE4D

Linked Data

• dbSNP Id: rs1817372276

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.59546958G>A , CM000667.2:g.59546958G>A	GRCh38
NC_000005.9:g.58842784G>A , CM000667.1:g.58842784G>A	GRCh37
NC_000005.8:g.58878541G>A	NCBI36
NG_027957.1:g.946142C>T
NG_027957.2:g.982372C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000507116.6:c.263+221289C>T	ENSP00000424852.1:n.263+221289C>T
ENST00000340635.11:c.456-330990C>T MANE Select	ENSP00000345502.6:n.456-330990C>T
ENST00000309641.10:c.263+221289C>T	ENSP00000308485.6:n.263+221289C>T
ENST00000340635.10:c.456-330990C>T	ENSP00000345502.6:n.456-330990C>T
ENST00000360047.9:c.47+39371C>T	ENSP00000353152.5:n.47+39371C>T
ENST00000405053.7:n.119-330990C>T
ENST00000502484.6:c.273-330990C>T	ENSP00000423094.2:n.273-330990C>T
ENST00000502575.1:c.263+221289C>T	ENSP00000425917.1:n.263+221289C>T
ENST00000505453.1:c.-99+39371C>T	ENSP00000421013.1:n.-99+39371C>T
ENST00000507116.5:c.263+221289C>T	ENSP00000424852.1:n.263+221289C>T
ENST00000514231.1:n.218+250102C>T
NM_001104631.1:c.456-330990C>T	NP_001098101.1:n.456-330990C>T
NM_001165899.1:c.273-330990C>T	NP_001159371.1:n.273-330990C>T
NM_001197218.1:c.263+221289C>T	NP_001184147.1:n.263+221289C>T
NM_006203.4:c.47+39371C>T	NP_006194.2:n.47+39371C>T
XM_005248538.3:c.47+39371C>T	XP_005248595.1:n.47+39371C>T
XM_011543469.1:c.420-330990C>T	XP_011541771.1:n.420-330990C>T
XM_011543470.1:c.420-330990C>T	XP_011541772.1:n.420-330990C>T
XM_011543471.1:c.273-330990C>T	XP_011541773.1:n.273-330990C>T
XM_011543472.1:c.273-330990C>T	XP_011541774.1:n.273-330990C>T
XM_011543473.1:c.273-330990C>T	XP_011541775.1:n.273-330990C>T
XM_011543474.1:c.243-330990C>T	XP_011541776.1:n.243-330990C>T
XM_011543477.1:c.14+250102C>T	XP_011541779.1:n.14+250102C>T
XM_011543478.1:c.-266+39371C>T	XP_011541780.1:n.-266+39371C>T
NM_001349241.1:c.243-330990C>T	NP_001336170.1:n.243-330990C>T
NM_001349242.1:c.-246+39371C>T	NP_001336171.1:n.-246+39371C>T
NM_001349243.1:c.-239-330990C>T	NP_001336172.1:n.-239-330990C>T
NM_001364599.1:c.273-330990C>T	NP_001351528.1:n.273-330990C>T
NM_001364600.1:c.273-330990C>T	NP_001351529.1:n.273-330990C>T
NM_001364601.1:c.263+221289C>T	NP_001351530.1:n.263+221289C>T
NM_001364602.1:c.263+221289C>T	NP_001351531.1:n.263+221289C>T
NM_001364603.1:c.-496+221289C>T	NP_001351532.1:n.-496+221289C>T
NM_001364604.1:c.-240+39371C>T	NP_001351533.1:n.-240+39371C>T
XM_011543470.2:c.420-330990C>T	XP_011541772.1:n.420-330990C>T
XM_011543471.2:c.273-330990C>T	XP_011541773.1:n.273-330990C>T
XM_017009565.1:c.420-330990C>T	XP_016865054.1:n.420-330990C>T
XM_017009566.1:c.273-330990C>T	XP_016865055.1:n.273-330990C>T
XM_017009567.1:c.258-330990C>T	XP_016865056.1:n.258-330990C>T
XM_024446110.1:c.420-330990C>T	XP_024301878.1:n.420-330990C>T
XM_024446112.1:c.273-330990C>T	XP_024301880.1:n.273-330990C>T
NM_001104631.2:c.456-330990C>T MANE Select	NP_001098101.1:n.456-330990C>T
NM_001165899.2:c.273-330990C>T	NP_001159371.1:n.273-330990C>T
NM_001197218.2:c.263+221289C>T	NP_001184147.1:n.263+221289C>T
NM_001349241.2:c.243-330990C>T	NP_001336170.1:n.243-330990C>T
NM_001349243.2:c.-239-330990C>T	NP_001336172.1:n.-239-330990C>T
NM_001364600.2:c.273-330990C>T	NP_001351529.1:n.273-330990C>T
NM_001364602.2:c.263+221289C>T	NP_001351531.1:n.263+221289C>T
NM_001349242.2:c.-246+39371C>T	NP_001336171.1:n.-246+39371C>T
NM_006203.5:c.47+39371C>T	NP_006194.2:n.47+39371C>T