Canonical Allele Identifier: CA359930545

Gene: PDE4D

Linked Data

• dbSNP Id: rs1744781836
• gnomAD v3: 5-59193535-G-A
• gnomAD v4: 5-59193535-G-A
• MyVariant Identifiers: chr5:g.58489361G>A (hg19) ; chr5:g.59193535G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.59193535G>A , CM000667.2:g.59193535G>A	GRCh38
NC_000005.9:g.58489361G>A , CM000667.1:g.58489361G>A	GRCh37
NC_000005.8:g.58525118G>A	NCBI36
NG_027957.1:g.1299565C>T
NG_027957.2:g.1335795C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507116.6:c.457C>T	ENSP00000424852.1:p.His153Tyr
ENST00000340635.11:c.649C>T MANE Select	ENSP00000345502.6:p.His217Tyr
ENST00000636120.1:c.319C>T	ENSP00000490821.1:p.His107Tyr
ENST00000638939.1:c.214C>T	ENSP00000492052.1:p.His72Tyr
ENST00000309641.10:c.457C>T	ENSP00000308485.6:p.His153Tyr
ENST00000340635.10:c.649C>T	ENSP00000345502.6:p.His217Tyr
ENST00000360047.9:c.241C>T	ENSP00000353152.5:p.His81Tyr
ENST00000405053.7:n.312C>T
ENST00000405755.6:c.283C>T	ENSP00000384806.2:p.His95Tyr
ENST00000502484.6:c.466C>T	ENSP00000423094.2:p.His156Tyr
ENST00000502575.1:c.457C>T	ENSP00000425917.1:p.His153Tyr
ENST00000503258.5:c.259C>T	ENSP00000425605.1:p.His87Tyr
ENST00000505453.1:c.-98-154564C>T	ENSP00000421013.1:n.-98-154564C>T
ENST00000507116.5:c.457C>T	ENSP00000424852.1:p.His153Tyr
ENST00000515324.1:n.161C>T
ENST00000546160.5:c.256C>T	ENSP00000442734.2:p.His86Tyr
ENST00000621323.4:n.194C>T
NM_001104631.1:c.649C>T	NP_001098101.1:p.His217Tyr
NM_001165899.1:c.466C>T	NP_001159371.1:p.His156Tyr
NM_001197218.1:c.457C>T	NP_001184147.1:p.His153Tyr
NM_001197219.1:c.283C>T	NP_001184148.1:p.His95Tyr
NM_001197220.1:c.259C>T	NP_001184149.1:p.His87Tyr
NM_006203.4:c.241C>T	NP_006194.2:p.His81Tyr
XM_005248537.2:c.319C>T	XP_005248594.1:p.His107Tyr
XM_005248538.3:c.241C>T	XP_005248595.1:p.His81Tyr
XM_011543469.1:c.613C>T	XP_011541771.1:p.His205Tyr
XM_011543470.1:c.613C>T	XP_011541772.1:p.His205Tyr
XM_011543471.1:c.466C>T	XP_011541773.1:p.His156Tyr
XM_011543472.1:c.466C>T	XP_011541774.1:p.His156Tyr
XM_011543473.1:c.466C>T	XP_011541775.1:p.His156Tyr
XM_011543474.1:c.436C>T	XP_011541776.1:p.His146Tyr
XM_011543475.1:c.283C>T	XP_011541777.1:p.His95Tyr
XM_011543476.1:c.229C>T	XP_011541778.1:p.His77Tyr
XM_011543477.1:c.208C>T	XP_011541779.1:p.His70Tyr
XM_011543478.1:c.145C>T	XP_011541780.1:p.His49Tyr
XM_011543479.1:c.145C>T	XP_011541781.1:p.His49Tyr
NM_001349241.1:c.436C>T	NP_001336170.1:p.His146Tyr
NM_001349242.1:c.319C>T	NP_001336171.1:p.His107Tyr
NM_001349243.1:c.-46C>T	NP_001336172.1:n.-46C>T
NM_001364599.1:c.466C>T	NP_001351528.1:p.His156Tyr
NM_001364600.1:c.466C>T	NP_001351529.1:p.His156Tyr
NM_001364602.1:c.457C>T	NP_001351531.1:p.His153Tyr
NM_001364603.1:c.-302C>T	NP_001351532.1:n.-302C>T
NM_001364604.1:c.-46C>T	NP_001351533.1:n.-46C>T
XM_011543470.2:c.613C>T	XP_011541772.1:p.His205Tyr
XM_011543471.2:c.466C>T	XP_011541773.1:p.His156Tyr
XM_017009565.1:c.613C>T	XP_016865054.1:p.His205Tyr
XM_017009566.1:c.466C>T	XP_016865055.1:p.His156Tyr
XM_017009567.1:c.451C>T	XP_016865056.1:p.His151Tyr
XM_024446110.1:c.613C>T	XP_024301878.1:p.His205Tyr
XM_024446112.1:c.466C>T	XP_024301880.1:p.His156Tyr
NM_001104631.2:c.649C>T MANE Select	NP_001098101.1:p.His217Tyr
NM_001165899.2:c.466C>T	NP_001159371.1:p.His156Tyr
NM_001197218.2:c.457C>T	NP_001184147.1:p.His153Tyr
NM_001197219.2:c.283C>T	NP_001184148.1:p.His95Tyr
NM_001197220.2:c.259C>T	NP_001184149.1:p.His87Tyr
NM_001349241.2:c.436C>T	NP_001336170.1:p.His146Tyr
NM_001349243.2:c.-46C>T	NP_001336172.1:n.-46C>T
NM_001364600.2:c.466C>T	NP_001351529.1:p.His156Tyr
NM_001364602.2:c.457C>T	NP_001351531.1:p.His153Tyr
NM_001349242.2:c.319C>T	NP_001336171.1:p.His107Tyr
NM_006203.5:c.241C>T	NP_006194.2:p.His81Tyr