Canonical Allele Identifier: CA119391771

Gene: PDE4D

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60143255T>A , CM000667.2:g.60143255T>A	GRCh38
NC_000005.9:g.59439082T>A , CM000667.1:g.59439082T>A	GRCh37
NC_000005.8:g.59474839T>A	NCBI36
NG_027957.1:g.349844A>T
NG_027957.2:g.386075A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502484.6:c.42+42302A>T	ENSP00000423094.2:n.42+42302A>T
ENST00000505507.6:c.42+42302A>T	ENSP00000425910.2:n.42+42302A>T
ENST00000506024.5:n.202+42302A>T
ENST00000506510.6:n.201+42302A>T
ENST00000509355.5:n.288+42302A>T
ENST00000509368.6:c.*184+4493A>T	ENSP00000423555.2:n.*184+4493A>T
ENST00000511382.1:n.304+42302A>T
ENST00000514552.5:c.42+42302A>T	ENSP00000421829.1:n.42+42302A>T
ENST00000515835.2:c.43-15574A>T	ENSP00000424281.2:n.43-15574A>T
NM_001165899.1:c.42+42302A>T	NP_001159371.1:n.42+42302A>T
XM_011543469.1:c.189+4493A>T	XP_011541771.1:n.189+4493A>T
XM_011543470.1:c.189+4493A>T	XP_011541772.1:n.189+4493A>T
XM_011543471.1:c.42+42302A>T	XP_011541773.1:n.42+42302A>T
XM_011543472.1:c.42+42302A>T	XP_011541774.1:n.42+42302A>T
XM_011543473.1:c.42+42302A>T	XP_011541775.1:n.42+42302A>T
XM_011543474.1:c.-62+42302A>T	XP_011541776.1:n.-62+42302A>T
NM_001349241.1:c.-62+42302A>T	NP_001336170.1:n.-62+42302A>T
NM_001349243.1:c.-543+42302A>T	NP_001336172.1:n.-543+42302A>T
NM_001364599.1:c.42+42302A>T	NP_001351528.1:n.42+42302A>T
NM_001364600.1:c.42+42302A>T	NP_001351529.1:n.42+42302A>T
XM_011543470.2:c.189+4493A>T	XP_011541772.1:n.189+4493A>T
XM_011543471.2:c.42+42302A>T	XP_011541773.1:n.42+42302A>T
XM_017009565.1:c.189+4493A>T	XP_016865054.1:n.189+4493A>T
XM_017009566.1:c.42+42302A>T	XP_016865055.1:n.42+42302A>T
XM_024446110.1:c.189+4493A>T	XP_024301878.1:n.189+4493A>T
XM_024446112.1:c.42+42302A>T	XP_024301880.1:n.42+42302A>T
NM_001165899.2:c.42+42302A>T	NP_001159371.1:n.42+42302A>T
NM_001349241.2:c.-62+42302A>T	NP_001336170.1:n.-62+42302A>T
NM_001349243.2:c.-543+42302A>T	NP_001336172.1:n.-543+42302A>T
NM_001364600.2:c.42+42302A>T	NP_001351529.1:n.42+42302A>T