Canonical Allele Identifier: CA1549618591

Gene: PDE4D

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60073967A= , CM000667.2:g.60073967A=	GRCh38
NC_000005.9:g.59369794A= , CM000667.1:g.59369794A=	GRCh37
NC_000005.8:g.59405551A=	NCBI36
NG_027957.1:g.419132T=
NG_027957.2:g.455363T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001165899.1:c.43-85250T=	NP_001159371.1:n.43-85250T=
NM_001165899.2:c.43-85250T=	NP_001159371.1:n.43-85250T=
NM_001349241.1:c.-61-69621T=	NP_001336170.1:n.-61-69621T=
NM_001349241.2:c.-61-69621T=	NP_001336170.1:n.-61-69621T=
NM_001349243.1:c.-542-69621T=	NP_001336172.1:n.-542-69621T=
NM_001349243.2:c.-542-69621T=	NP_001336172.1:n.-542-69621T=
NM_001364599.1:c.43-85250T=	NP_001351528.1:n.43-85250T=
NM_001364600.1:c.43-85250T=	NP_001351529.1:n.43-85250T=
NM_001364600.2:c.43-85250T=	NP_001351529.1:n.43-85250T=
ENST00000502484.6:c.43-85250T=	ENSP00000423094.2:n.43-85250T=
ENST00000505507.6:c.43-85250T=	ENSP00000425910.2:n.43-85250T=
ENST00000506024.5:n.203-85250T=
ENST00000506510.6:n.202-85250T=
ENST00000509355.5:n.289-85250T=
ENST00000509368.6:c.*184+73781T=	ENSP00000423555.2:n.*184+73781T=
ENST00000511382.1:n.305-85250T=
ENST00000514552.5:c.43-85250T=	ENSP00000421829.1:n.43-85250T=
ENST00000515835.2:c.*50+53617T=	ENSP00000424281.2:n.*50+53617T=
XM_011543469.1:c.189+73781T=	XP_011541771.1:n.189+73781T=
XM_011543470.1:c.189+73781T=	XP_011541772.1:n.189+73781T=
XM_011543470.2:c.189+73781T=	XP_011541772.1:n.189+73781T=
XM_011543471.1:c.43-85250T=	XP_011541773.1:n.43-85250T=
XM_011543471.2:c.43-85250T=	XP_011541773.1:n.43-85250T=
XM_011543472.1:c.43-85250T=	XP_011541774.1:n.43-85250T=
XM_011543473.1:c.43-85250T=	XP_011541775.1:n.43-85250T=
XM_011543474.1:c.-61-69621T=	XP_011541776.1:n.-61-69621T=
XM_017009565.1:c.189+73781T=	XP_016865054.1:n.189+73781T=
XM_017009566.1:c.43-85250T=	XP_016865055.1:n.43-85250T=
XM_024446110.1:c.189+73781T=	XP_024301878.1:n.189+73781T=
XM_024446112.1:c.43-85250T=	XP_024301880.1:n.43-85250T=