Canonical Allele Identifier: CA1549122359

Gene: PDE4D

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.58976421T= , CM000667.2:g.58976421T=	GRCh38
NC_000005.9:g.58272248T= , CM000667.1:g.58272248T=	GRCh37
NC_000005.8:g.58308005T=	NCBI36
NG_027957.1:g.1516678A=
NG_027957.2:g.1552909A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507116.6:c.1567A=	ENSP00000424852.1:p.Thr523=
ENST00000340635.11:c.1759A= MANE Select	ENSP00000345502.6:p.Thr587=
ENST00000636120.1:c.1429A=	ENSP00000490821.1:p.Thr477=
ENST00000309641.10:c.1611A=	ENSP00000308485.6:n.1611A=
ENST00000317118.12:c.886A=	ENSP00000321739.8:p.Thr296=
ENST00000340635.10:c.1759A=	ENSP00000345502.6:p.Thr587=
ENST00000358923.10:c.853A=	ENSP00000351800.6:p.Thr285=
ENST00000360047.9:c.1351A=	ENSP00000353152.5:p.Thr451=
ENST00000405755.6:c.1393A=	ENSP00000384806.2:p.Thr465=
ENST00000502484.6:c.1576A=	ENSP00000423094.2:p.Thr526=
ENST00000503258.5:c.1369A=	ENSP00000425605.1:p.Thr457=
ENST00000505453.1:c.853A=	ENSP00000421013.1:p.Thr285=
ENST00000507116.5:c.1567A=	ENSP00000424852.1:p.Thr523=
ENST00000515011.5:n.1495A=
ENST00000546160.5:c.1366A=	ENSP00000442734.2:p.Thr456=
NM_001104631.1:c.1759A=	NP_001098101.1:p.Thr587=
NM_001165899.1:c.1576A=	NP_001159371.1:p.Thr526=
NM_001197218.1:c.1567A=	NP_001184147.1:p.Thr523=
NM_001197219.1:c.1393A=	NP_001184148.1:p.Thr465=
NM_001197220.1:c.1369A=	NP_001184149.1:p.Thr457=
NM_001197221.1:c.853A=	NP_001184150.1:p.Thr285=
NM_001197222.1:c.1087A=	NP_001184151.1:p.Thr363=
NM_001197223.1:c.886A=	NP_001184152.1:p.Thr296=
NM_006203.4:c.1351A=	NP_006194.2:p.Thr451=
XM_005248537.2:c.1429A=	XP_005248594.1:p.Thr477=
XM_005248538.3:c.1351A=	XP_005248595.1:p.Thr451=
XM_011543469.1:c.1723A=	XP_011541771.1:p.Thr575=
XM_011543470.1:c.1723A=	XP_011541772.1:p.Thr575=
XM_011543471.1:c.1576A=	XP_011541773.1:p.Thr526=
XM_011543472.1:c.1576A=	XP_011541774.1:p.Thr526=
XM_011543473.1:c.1576A=	XP_011541775.1:p.Thr526=
XM_011543474.1:c.1546A=	XP_011541776.1:p.Thr516=
XM_011543475.1:c.1393A=	XP_011541777.1:p.Thr465=
XM_011543476.1:c.1339A=	XP_011541778.1:p.Thr447=
XM_011543477.1:c.1318A=	XP_011541779.1:p.Thr440=
XM_011543478.1:c.1255A=	XP_011541780.1:p.Thr419=
XM_011543479.1:c.1255A=	XP_011541781.1:p.Thr419=
NM_001349241.1:c.1546A=	NP_001336170.1:p.Thr516=
NM_001349242.1:c.1429A=	NP_001336171.1:p.Thr477=
NM_001349243.1:c.991A=	NP_001336172.1:p.Thr331=
NM_001364599.1:c.1576A=	NP_001351528.1:p.Thr526=
NM_001364603.1:c.853A=	NP_001351532.1:p.Thr285=
NM_001364604.1:c.991A=	NP_001351533.1:p.Thr331=
XM_011543470.2:c.1723A=	XP_011541772.1:p.Thr575=
XM_011543471.2:c.1576A=	XP_011541773.1:p.Thr526=
XM_017009565.1:c.1723A=	XP_016865054.1:p.Thr575=
XM_017009566.1:c.1576A=	XP_016865055.1:p.Thr526=
XM_017009567.1:c.1561A=	XP_016865056.1:p.Thr521=
XM_024446110.1:c.1723A=	XP_024301878.1:p.Thr575=
XM_024446112.1:c.1576A=	XP_024301880.1:p.Thr526=
NM_001104631.2:c.1759A= MANE Select	NP_001098101.1:p.Thr587=
NM_001165899.2:c.1576A=	NP_001159371.1:p.Thr526=
NM_001197218.2:c.1567A=	NP_001184147.1:p.Thr523=
NM_001197219.2:c.1393A=	NP_001184148.1:p.Thr465=
NM_001197220.2:c.1369A=	NP_001184149.1:p.Thr457=
NM_001197221.2:c.853A=	NP_001184150.1:p.Thr285=
NM_001197222.2:c.1087A=	NP_001184151.1:p.Thr363=
NM_001197223.2:c.886A=	NP_001184152.1:p.Thr296=
NM_001349241.2:c.1546A=	NP_001336170.1:p.Thr516=
NM_001349243.2:c.991A=	NP_001336172.1:p.Thr331=
NM_001349242.2:c.1429A=	NP_001336171.1:p.Thr477=
NM_006203.5:c.1351A=	NP_006194.2:p.Thr451=