Canonical Allele Identifier: CA359930871

Gene: PDE4D

Linked Data

• MyVariant Identifiers: chr5:g.58511672T>G (hg19) ; chr5:g.59215846T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.59215846T>G , CM000667.2:g.59215846T>G	GRCh38
NC_000005.9:g.58511672T>G , CM000667.1:g.58511672T>G	GRCh37
NC_000005.8:g.58547429T>G	NCBI36
NG_027957.1:g.1277254A>C
NG_027957.2:g.1313484A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507116.6:c.386A>C	ENSP00000424852.1:p.Tyr129Ser
ENST00000340635.11:c.578A>C MANE Select	ENSP00000345502.6:p.Tyr193Ser
ENST00000636120.1:c.248A>C	ENSP00000490821.1:p.Tyr83Ser
ENST00000638939.1:c.143A>C	ENSP00000492052.1:p.Tyr48Ser
ENST00000309641.10:c.386A>C	ENSP00000308485.6:p.Tyr129Ser
ENST00000340635.10:c.578A>C	ENSP00000345502.6:p.Tyr193Ser
ENST00000360047.9:c.170A>C	ENSP00000353152.5:p.Tyr57Ser
ENST00000405053.7:n.241A>C
ENST00000405755.6:c.212A>C	ENSP00000384806.2:p.Tyr71Ser
ENST00000502484.6:c.395A>C	ENSP00000423094.2:p.Tyr132Ser
ENST00000502575.1:c.386A>C	ENSP00000425917.1:p.Tyr129Ser
ENST00000503258.5:c.188A>C	ENSP00000425605.1:p.Tyr63Ser
ENST00000505453.1:c.-98-176875A>C	ENSP00000421013.1:n.-98-176875A>C
ENST00000507116.5:c.386A>C	ENSP00000424852.1:p.Tyr129Ser
ENST00000514231.1:n.341A>C
ENST00000515324.1:n.90A>C
ENST00000546160.5:c.185A>C	ENSP00000442734.2:p.Tyr62Ser
ENST00000621323.4:n.123A>C
NM_001104631.1:c.578A>C	NP_001098101.1:p.Tyr193Ser
NM_001165899.1:c.395A>C	NP_001159371.1:p.Tyr132Ser
NM_001197218.1:c.386A>C	NP_001184147.1:p.Tyr129Ser
NM_001197219.1:c.212A>C	NP_001184148.1:p.Tyr71Ser
NM_001197220.1:c.188A>C	NP_001184149.1:p.Tyr63Ser
NM_006203.4:c.170A>C	NP_006194.2:p.Tyr57Ser
XM_005248537.2:c.248A>C	XP_005248594.1:p.Tyr83Ser
XM_005248538.3:c.170A>C	XP_005248595.1:p.Tyr57Ser
XM_011543469.1:c.542A>C	XP_011541771.1:p.Tyr181Ser
XM_011543470.1:c.542A>C	XP_011541772.1:p.Tyr181Ser
XM_011543471.1:c.395A>C	XP_011541773.1:p.Tyr132Ser
XM_011543472.1:c.395A>C	XP_011541774.1:p.Tyr132Ser
XM_011543473.1:c.395A>C	XP_011541775.1:p.Tyr132Ser
XM_011543474.1:c.365A>C	XP_011541776.1:p.Tyr122Ser
XM_011543475.1:c.212A>C	XP_011541777.1:p.Tyr71Ser
XM_011543476.1:c.158A>C	XP_011541778.1:p.Tyr53Ser
XM_011543477.1:c.137A>C	XP_011541779.1:p.Tyr46Ser
XM_011543478.1:c.74A>C	XP_011541780.1:p.Tyr25Ser
XM_011543479.1:c.74A>C	XP_011541781.1:p.Tyr25Ser
NM_001349241.1:c.365A>C	NP_001336170.1:p.Tyr122Ser
NM_001349242.1:c.248A>C	NP_001336171.1:p.Tyr83Ser
NM_001349243.1:c.-117A>C	NP_001336172.1:n.-117A>C
NM_001364599.1:c.395A>C	NP_001351528.1:p.Tyr132Ser
NM_001364600.1:c.395A>C	NP_001351529.1:p.Tyr132Ser
NM_001364601.1:c.386A>C	NP_001351530.1:p.Tyr129Ser
NM_001364602.1:c.386A>C	NP_001351531.1:p.Tyr129Ser
NM_001364603.1:c.-373A>C	NP_001351532.1:n.-373A>C
NM_001364604.1:c.-117A>C	NP_001351533.1:n.-117A>C
XM_011543470.2:c.542A>C	XP_011541772.1:p.Tyr181Ser
XM_011543471.2:c.395A>C	XP_011541773.1:p.Tyr132Ser
XM_017009565.1:c.542A>C	XP_016865054.1:p.Tyr181Ser
XM_017009566.1:c.395A>C	XP_016865055.1:p.Tyr132Ser
XM_017009567.1:c.380A>C	XP_016865056.1:p.Tyr127Ser
XM_024446110.1:c.542A>C	XP_024301878.1:p.Tyr181Ser
XM_024446112.1:c.395A>C	XP_024301880.1:p.Tyr132Ser
NM_001104631.2:c.578A>C MANE Select	NP_001098101.1:p.Tyr193Ser
NM_001165899.2:c.395A>C	NP_001159371.1:p.Tyr132Ser
NM_001197218.2:c.386A>C	NP_001184147.1:p.Tyr129Ser
NM_001197219.2:c.212A>C	NP_001184148.1:p.Tyr71Ser
NM_001197220.2:c.188A>C	NP_001184149.1:p.Tyr63Ser
NM_001349241.2:c.365A>C	NP_001336170.1:p.Tyr122Ser
NM_001349243.2:c.-117A>C	NP_001336172.1:n.-117A>C
NM_001364600.2:c.395A>C	NP_001351529.1:p.Tyr132Ser
NM_001364602.2:c.386A>C	NP_001351531.1:p.Tyr129Ser
NM_001349242.2:c.248A>C	NP_001336171.1:p.Tyr83Ser
NM_006203.5:c.170A>C	NP_006194.2:p.Tyr57Ser