Canonical Allele Identifier: CA444501198

Gene: PDE4D

Linked Data

• MyVariant Identifiers: chr5:g.58489344A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.59193518A>T , CM000667.2:g.59193518A>T	GRCh38
NC_000005.9:g.58489344A>T , CM000667.1:g.58489344A>T	GRCh37
NC_000005.8:g.58525101A>T	NCBI36
NG_027957.1:g.1299582T>A
NG_027957.2:g.1335812T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507116.6:c.474T>A	ENSP00000424852.1:p.Ile158=
ENST00000340635.11:c.666T>A MANE Select	ENSP00000345502.6:p.Ile222=
ENST00000636120.1:c.336T>A	ENSP00000490821.1:p.Ile112=
ENST00000638939.1:c.231T>A	ENSP00000492052.1:p.Ile77=
ENST00000309641.10:c.474T>A	ENSP00000308485.6:p.Ile158=
ENST00000340635.10:c.666T>A	ENSP00000345502.6:p.Ile222=
ENST00000360047.9:c.258T>A	ENSP00000353152.5:p.Ile86=
ENST00000405053.7:n.329T>A
ENST00000405755.6:c.300T>A	ENSP00000384806.2:p.Ile100=
ENST00000502484.6:c.483T>A	ENSP00000423094.2:p.Ile161=
ENST00000502575.1:c.474T>A	ENSP00000425917.1:p.Ile158=
ENST00000503258.5:c.276T>A	ENSP00000425605.1:p.Ile92=
ENST00000505453.1:c.-98-154547T>A	ENSP00000421013.1:n.-98-154547T>A
ENST00000507116.5:c.474T>A	ENSP00000424852.1:p.Ile158=
ENST00000515324.1:n.178T>A
ENST00000546160.5:c.273T>A	ENSP00000442734.2:p.Ile91=
ENST00000621323.4:n.211T>A
NM_001104631.1:c.666T>A	NP_001098101.1:p.Ile222=
NM_001165899.1:c.483T>A	NP_001159371.1:p.Ile161=
NM_001197218.1:c.474T>A	NP_001184147.1:p.Ile158=
NM_001197219.1:c.300T>A	NP_001184148.1:p.Ile100=
NM_001197220.1:c.276T>A	NP_001184149.1:p.Ile92=
NM_006203.4:c.258T>A	NP_006194.2:p.Ile86=
XM_005248537.2:c.336T>A	XP_005248594.1:p.Ile112=
XM_005248538.3:c.258T>A	XP_005248595.1:p.Ile86=
XM_011543469.1:c.630T>A	XP_011541771.1:p.Ile210=
XM_011543470.1:c.630T>A	XP_011541772.1:p.Ile210=
XM_011543471.1:c.483T>A	XP_011541773.1:p.Ile161=
XM_011543472.1:c.483T>A	XP_011541774.1:p.Ile161=
XM_011543473.1:c.483T>A	XP_011541775.1:p.Ile161=
XM_011543474.1:c.453T>A	XP_011541776.1:p.Ile151=
XM_011543475.1:c.300T>A	XP_011541777.1:p.Ile100=
XM_011543476.1:c.246T>A	XP_011541778.1:p.Ile82=
XM_011543477.1:c.225T>A	XP_011541779.1:p.Ile75=
XM_011543478.1:c.162T>A	XP_011541780.1:p.Ile54=
XM_011543479.1:c.162T>A	XP_011541781.1:p.Ile54=
NM_001349241.1:c.453T>A	NP_001336170.1:p.Ile151=
NM_001349242.1:c.336T>A	NP_001336171.1:p.Ile112=
NM_001349243.1:c.-29T>A	NP_001336172.1:n.-29T>A
NM_001364599.1:c.483T>A	NP_001351528.1:p.Ile161=
NM_001364600.1:c.483T>A	NP_001351529.1:p.Ile161=
NM_001364602.1:c.474T>A	NP_001351531.1:p.Ile158=
NM_001364603.1:c.-285T>A	NP_001351532.1:n.-285T>A
NM_001364604.1:c.-29T>A	NP_001351533.1:n.-29T>A
XM_011543470.2:c.630T>A	XP_011541772.1:p.Ile210=
XM_011543471.2:c.483T>A	XP_011541773.1:p.Ile161=
XM_017009565.1:c.630T>A	XP_016865054.1:p.Ile210=
XM_017009566.1:c.483T>A	XP_016865055.1:p.Ile161=
XM_017009567.1:c.468T>A	XP_016865056.1:p.Ile156=
XM_024446110.1:c.630T>A	XP_024301878.1:p.Ile210=
XM_024446112.1:c.483T>A	XP_024301880.1:p.Ile161=
NM_001104631.2:c.666T>A MANE Select	NP_001098101.1:p.Ile222=
NM_001165899.2:c.483T>A	NP_001159371.1:p.Ile161=
NM_001197218.2:c.474T>A	NP_001184147.1:p.Ile158=
NM_001197219.2:c.300T>A	NP_001184148.1:p.Ile100=
NM_001197220.2:c.276T>A	NP_001184149.1:p.Ile92=
NM_001349241.2:c.453T>A	NP_001336170.1:p.Ile151=
NM_001349243.2:c.-29T>A	NP_001336172.1:n.-29T>A
NM_001364600.2:c.483T>A	NP_001351529.1:p.Ile161=
NM_001364602.2:c.474T>A	NP_001351531.1:p.Ile158=
NM_001349242.2:c.336T>A	NP_001336171.1:p.Ile112=
NM_006203.5:c.258T>A	NP_006194.2:p.Ile86=