Canonical Allele Identifier: CA1549229323

Gene: PDE4D

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.59215838C= , CM000667.2:g.59215838C=	GRCh38
NC_000005.9:g.58511664C= , CM000667.1:g.58511664C=	GRCh37
NC_000005.8:g.58547421C=	NCBI36
NG_027957.1:g.1277262G=
NG_027957.2:g.1313492G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507116.6:c.394G=	ENSP00000424852.1:p.Asp132=
ENST00000340635.11:c.586G= MANE Select	ENSP00000345502.6:p.Asp196=
ENST00000636120.1:c.256G=	ENSP00000490821.1:p.Asp86=
ENST00000638939.1:c.151G=	ENSP00000492052.1:p.Asp51=
ENST00000309641.10:c.394G=	ENSP00000308485.6:p.Asp132=
ENST00000340635.10:c.586G=	ENSP00000345502.6:p.Asp196=
ENST00000360047.9:c.178G=	ENSP00000353152.5:p.Asp60=
ENST00000405053.7:n.249G=
ENST00000405755.6:c.220G=	ENSP00000384806.2:p.Asp74=
ENST00000502484.6:c.403G=	ENSP00000423094.2:p.Asp135=
ENST00000502575.1:c.394G=	ENSP00000425917.1:p.Asp132=
ENST00000503258.5:c.196G=	ENSP00000425605.1:p.Asp66=
ENST00000505453.1:c.-98-176867G=	ENSP00000421013.1:n.-98-176867G=
ENST00000507116.5:c.394G=	ENSP00000424852.1:p.Asp132=
ENST00000514231.1:n.349G=
ENST00000515324.1:n.98G=
ENST00000546160.5:c.193G=	ENSP00000442734.2:p.Asp65=
ENST00000621323.4:n.131G=
NM_001104631.1:c.586G=	NP_001098101.1:p.Asp196=
NM_001165899.1:c.403G=	NP_001159371.1:p.Asp135=
NM_001197218.1:c.394G=	NP_001184147.1:p.Asp132=
NM_001197219.1:c.220G=	NP_001184148.1:p.Asp74=
NM_001197220.1:c.196G=	NP_001184149.1:p.Asp66=
NM_006203.4:c.178G=	NP_006194.2:p.Asp60=
XM_005248537.2:c.256G=	XP_005248594.1:p.Asp86=
XM_005248538.3:c.178G=	XP_005248595.1:p.Asp60=
XM_011543469.1:c.550G=	XP_011541771.1:p.Asp184=
XM_011543470.1:c.550G=	XP_011541772.1:p.Asp184=
XM_011543471.1:c.403G=	XP_011541773.1:p.Asp135=
XM_011543472.1:c.403G=	XP_011541774.1:p.Asp135=
XM_011543473.1:c.403G=	XP_011541775.1:p.Asp135=
XM_011543474.1:c.373G=	XP_011541776.1:p.Asp125=
XM_011543475.1:c.220G=	XP_011541777.1:p.Asp74=
XM_011543476.1:c.166G=	XP_011541778.1:p.Asp56=
XM_011543477.1:c.145G=	XP_011541779.1:p.Asp49=
XM_011543478.1:c.82G=	XP_011541780.1:p.Asp28=
XM_011543479.1:c.82G=	XP_011541781.1:p.Asp28=
NM_001349241.1:c.373G=	NP_001336170.1:p.Asp125=
NM_001349242.1:c.256G=	NP_001336171.1:p.Asp86=
NM_001349243.1:c.-109G=	NP_001336172.1:n.-109G=
NM_001364599.1:c.403G=	NP_001351528.1:p.Asp135=
NM_001364600.1:c.403G=	NP_001351529.1:p.Asp135=
NM_001364601.1:c.394G=	NP_001351530.1:p.Asp132=
NM_001364602.1:c.394G=	NP_001351531.1:p.Asp132=
NM_001364603.1:c.-365G=	NP_001351532.1:n.-365G=
NM_001364604.1:c.-109G=	NP_001351533.1:n.-109G=
XM_011543470.2:c.550G=	XP_011541772.1:p.Asp184=
XM_011543471.2:c.403G=	XP_011541773.1:p.Asp135=
XM_017009565.1:c.550G=	XP_016865054.1:p.Asp184=
XM_017009566.1:c.403G=	XP_016865055.1:p.Asp135=
XM_017009567.1:c.388G=	XP_016865056.1:p.Asp130=
XM_024446110.1:c.550G=	XP_024301878.1:p.Asp184=
XM_024446112.1:c.403G=	XP_024301880.1:p.Asp135=
NM_001104631.2:c.586G= MANE Select	NP_001098101.1:p.Asp196=
NM_001165899.2:c.403G=	NP_001159371.1:p.Asp135=
NM_001197218.2:c.394G=	NP_001184147.1:p.Asp132=
NM_001197219.2:c.220G=	NP_001184148.1:p.Asp74=
NM_001197220.2:c.196G=	NP_001184149.1:p.Asp66=
NM_001349241.2:c.373G=	NP_001336170.1:p.Asp125=
NM_001349243.2:c.-109G=	NP_001336172.1:n.-109G=
NM_001364600.2:c.403G=	NP_001351529.1:p.Asp135=
NM_001364602.2:c.394G=	NP_001351531.1:p.Asp132=
NM_001349242.2:c.256G=	NP_001336171.1:p.Asp86=
NM_006203.5:c.178G=	NP_006194.2:p.Asp60=