Canonical Allele Identifier: CA359930506

Gene: PDE4D

Linked Data

• MyVariant Identifiers: chr5:g.58489345A>C (hg19) ; chr5:g.59193519A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.59193519A>C , CM000667.2:g.59193519A>C	GRCh38
NC_000005.9:g.58489345A>C , CM000667.1:g.58489345A>C	GRCh37
NC_000005.8:g.58525102A>C	NCBI36
NG_027957.1:g.1299581T>G
NG_027957.2:g.1335811T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507116.6:c.473T>G	ENSP00000424852.1:p.Ile158Ser
ENST00000340635.11:c.665T>G MANE Select	ENSP00000345502.6:p.Ile222Ser
ENST00000636120.1:c.335T>G	ENSP00000490821.1:p.Ile112Ser
ENST00000638939.1:c.230T>G	ENSP00000492052.1:p.Ile77Ser
ENST00000309641.10:c.473T>G	ENSP00000308485.6:p.Ile158Ser
ENST00000340635.10:c.665T>G	ENSP00000345502.6:p.Ile222Ser
ENST00000360047.9:c.257T>G	ENSP00000353152.5:p.Ile86Ser
ENST00000405053.7:n.328T>G
ENST00000405755.6:c.299T>G	ENSP00000384806.2:p.Ile100Ser
ENST00000502484.6:c.482T>G	ENSP00000423094.2:p.Ile161Ser
ENST00000502575.1:c.473T>G	ENSP00000425917.1:p.Ile158Ser
ENST00000503258.5:c.275T>G	ENSP00000425605.1:p.Ile92Ser
ENST00000505453.1:c.-98-154548T>G	ENSP00000421013.1:n.-98-154548T>G
ENST00000507116.5:c.473T>G	ENSP00000424852.1:p.Ile158Ser
ENST00000515324.1:n.177T>G
ENST00000546160.5:c.272T>G	ENSP00000442734.2:p.Ile91Ser
ENST00000621323.4:n.210T>G
NM_001104631.1:c.665T>G	NP_001098101.1:p.Ile222Ser
NM_001165899.1:c.482T>G	NP_001159371.1:p.Ile161Ser
NM_001197218.1:c.473T>G	NP_001184147.1:p.Ile158Ser
NM_001197219.1:c.299T>G	NP_001184148.1:p.Ile100Ser
NM_001197220.1:c.275T>G	NP_001184149.1:p.Ile92Ser
NM_006203.4:c.257T>G	NP_006194.2:p.Ile86Ser
XM_005248537.2:c.335T>G	XP_005248594.1:p.Ile112Ser
XM_005248538.3:c.257T>G	XP_005248595.1:p.Ile86Ser
XM_011543469.1:c.629T>G	XP_011541771.1:p.Ile210Ser
XM_011543470.1:c.629T>G	XP_011541772.1:p.Ile210Ser
XM_011543471.1:c.482T>G	XP_011541773.1:p.Ile161Ser
XM_011543472.1:c.482T>G	XP_011541774.1:p.Ile161Ser
XM_011543473.1:c.482T>G	XP_011541775.1:p.Ile161Ser
XM_011543474.1:c.452T>G	XP_011541776.1:p.Ile151Ser
XM_011543475.1:c.299T>G	XP_011541777.1:p.Ile100Ser
XM_011543476.1:c.245T>G	XP_011541778.1:p.Ile82Ser
XM_011543477.1:c.224T>G	XP_011541779.1:p.Ile75Ser
XM_011543478.1:c.161T>G	XP_011541780.1:p.Ile54Ser
XM_011543479.1:c.161T>G	XP_011541781.1:p.Ile54Ser
NM_001349241.1:c.452T>G	NP_001336170.1:p.Ile151Ser
NM_001349242.1:c.335T>G	NP_001336171.1:p.Ile112Ser
NM_001349243.1:c.-30T>G	NP_001336172.1:n.-30T>G
NM_001364599.1:c.482T>G	NP_001351528.1:p.Ile161Ser
NM_001364600.1:c.482T>G	NP_001351529.1:p.Ile161Ser
NM_001364602.1:c.473T>G	NP_001351531.1:p.Ile158Ser
NM_001364603.1:c.-286T>G	NP_001351532.1:n.-286T>G
NM_001364604.1:c.-30T>G	NP_001351533.1:n.-30T>G
XM_011543470.2:c.629T>G	XP_011541772.1:p.Ile210Ser
XM_011543471.2:c.482T>G	XP_011541773.1:p.Ile161Ser
XM_017009565.1:c.629T>G	XP_016865054.1:p.Ile210Ser
XM_017009566.1:c.482T>G	XP_016865055.1:p.Ile161Ser
XM_017009567.1:c.467T>G	XP_016865056.1:p.Ile156Ser
XM_024446110.1:c.629T>G	XP_024301878.1:p.Ile210Ser
XM_024446112.1:c.482T>G	XP_024301880.1:p.Ile161Ser
NM_001104631.2:c.665T>G MANE Select	NP_001098101.1:p.Ile222Ser
NM_001165899.2:c.482T>G	NP_001159371.1:p.Ile161Ser
NM_001197218.2:c.473T>G	NP_001184147.1:p.Ile158Ser
NM_001197219.2:c.299T>G	NP_001184148.1:p.Ile100Ser
NM_001197220.2:c.275T>G	NP_001184149.1:p.Ile92Ser
NM_001349241.2:c.452T>G	NP_001336170.1:p.Ile151Ser
NM_001349243.2:c.-30T>G	NP_001336172.1:n.-30T>G
NM_001364600.2:c.482T>G	NP_001351529.1:p.Ile161Ser
NM_001364602.2:c.473T>G	NP_001351531.1:p.Ile158Ser
NM_001349242.2:c.335T>G	NP_001336171.1:p.Ile112Ser
NM_006203.5:c.257T>G	NP_006194.2:p.Ile86Ser