Canonical Allele Identifier: CA359930529

Gene: PDE4D

Linked Data

• gnomAD v3: 5-59193528-T-A
• gnomAD v4: 5-59193528-T-A
• MyVariant Identifiers: chr5:g.58489354T>A (hg19) ; chr5:g.59193528T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.59193528T>A , CM000667.2:g.59193528T>A	GRCh38
NC_000005.9:g.58489354T>A , CM000667.1:g.58489354T>A	GRCh37
NC_000005.8:g.58525111T>A	NCBI36
NG_027957.1:g.1299572A>T
NG_027957.2:g.1335802A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507116.6:c.464A>T	ENSP00000424852.1:p.Asp155Val
ENST00000340635.11:c.656A>T MANE Select	ENSP00000345502.6:p.Asp219Val
ENST00000636120.1:c.326A>T	ENSP00000490821.1:p.Asp109Val
ENST00000638939.1:c.221A>T	ENSP00000492052.1:p.Asp74Val
ENST00000309641.10:c.464A>T	ENSP00000308485.6:p.Asp155Val
ENST00000340635.10:c.656A>T	ENSP00000345502.6:p.Asp219Val
ENST00000360047.9:c.248A>T	ENSP00000353152.5:p.Asp83Val
ENST00000405053.7:n.319A>T
ENST00000405755.6:c.290A>T	ENSP00000384806.2:p.Asp97Val
ENST00000502484.6:c.473A>T	ENSP00000423094.2:p.Asp158Val
ENST00000502575.1:c.464A>T	ENSP00000425917.1:p.Asp155Val
ENST00000503258.5:c.266A>T	ENSP00000425605.1:p.Asp89Val
ENST00000505453.1:c.-98-154557A>T	ENSP00000421013.1:n.-98-154557A>T
ENST00000507116.5:c.464A>T	ENSP00000424852.1:p.Asp155Val
ENST00000515324.1:n.168A>T
ENST00000546160.5:c.263A>T	ENSP00000442734.2:p.Asp88Val
ENST00000621323.4:n.201A>T
NM_001104631.1:c.656A>T	NP_001098101.1:p.Asp219Val
NM_001165899.1:c.473A>T	NP_001159371.1:p.Asp158Val
NM_001197218.1:c.464A>T	NP_001184147.1:p.Asp155Val
NM_001197219.1:c.290A>T	NP_001184148.1:p.Asp97Val
NM_001197220.1:c.266A>T	NP_001184149.1:p.Asp89Val
NM_006203.4:c.248A>T	NP_006194.2:p.Asp83Val
XM_005248537.2:c.326A>T	XP_005248594.1:p.Asp109Val
XM_005248538.3:c.248A>T	XP_005248595.1:p.Asp83Val
XM_011543469.1:c.620A>T	XP_011541771.1:p.Asp207Val
XM_011543470.1:c.620A>T	XP_011541772.1:p.Asp207Val
XM_011543471.1:c.473A>T	XP_011541773.1:p.Asp158Val
XM_011543472.1:c.473A>T	XP_011541774.1:p.Asp158Val
XM_011543473.1:c.473A>T	XP_011541775.1:p.Asp158Val
XM_011543474.1:c.443A>T	XP_011541776.1:p.Asp148Val
XM_011543475.1:c.290A>T	XP_011541777.1:p.Asp97Val
XM_011543476.1:c.236A>T	XP_011541778.1:p.Asp79Val
XM_011543477.1:c.215A>T	XP_011541779.1:p.Asp72Val
XM_011543478.1:c.152A>T	XP_011541780.1:p.Asp51Val
XM_011543479.1:c.152A>T	XP_011541781.1:p.Asp51Val
NM_001349241.1:c.443A>T	NP_001336170.1:p.Asp148Val
NM_001349242.1:c.326A>T	NP_001336171.1:p.Asp109Val
NM_001349243.1:c.-39A>T	NP_001336172.1:n.-39A>T
NM_001364599.1:c.473A>T	NP_001351528.1:p.Asp158Val
NM_001364600.1:c.473A>T	NP_001351529.1:p.Asp158Val
NM_001364602.1:c.464A>T	NP_001351531.1:p.Asp155Val
NM_001364603.1:c.-295A>T	NP_001351532.1:n.-295A>T
NM_001364604.1:c.-39A>T	NP_001351533.1:n.-39A>T
XM_011543470.2:c.620A>T	XP_011541772.1:p.Asp207Val
XM_011543471.2:c.473A>T	XP_011541773.1:p.Asp158Val
XM_017009565.1:c.620A>T	XP_016865054.1:p.Asp207Val
XM_017009566.1:c.473A>T	XP_016865055.1:p.Asp158Val
XM_017009567.1:c.458A>T	XP_016865056.1:p.Asp153Val
XM_024446110.1:c.620A>T	XP_024301878.1:p.Asp207Val
XM_024446112.1:c.473A>T	XP_024301880.1:p.Asp158Val
NM_001104631.2:c.656A>T MANE Select	NP_001098101.1:p.Asp219Val
NM_001165899.2:c.473A>T	NP_001159371.1:p.Asp158Val
NM_001197218.2:c.464A>T	NP_001184147.1:p.Asp155Val
NM_001197219.2:c.290A>T	NP_001184148.1:p.Asp97Val
NM_001197220.2:c.266A>T	NP_001184149.1:p.Asp89Val
NM_001349241.2:c.443A>T	NP_001336170.1:p.Asp148Val
NM_001349243.2:c.-39A>T	NP_001336172.1:n.-39A>T
NM_001364600.2:c.473A>T	NP_001351529.1:p.Asp158Val
NM_001364602.2:c.464A>T	NP_001351531.1:p.Asp155Val
NM_001349242.2:c.326A>T	NP_001336171.1:p.Asp109Val
NM_006203.5:c.248A>T	NP_006194.2:p.Asp83Val