Canonical Allele Identifier: CA3276120

Gene: PDE4D

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.58990906G>C , CM000667.2:g.58990906G>C	GRCh38
NC_000005.9:g.58286733G>C , CM000667.1:g.58286733G>C	GRCh37
NC_000005.8:g.58322490G>C	NCBI36
NG_027957.1:g.1502193C>G
NG_027957.2:g.1538424C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001104631.2:c.1189-4C>G MANE Select	NP_001098101.1:n.1189-4C>G
ENST00000340635.11:c.1189-4C>G MANE Select	ENSP00000345502.6:n.1189-4C>G
NM_001104631.1:c.1189-4C>G	NP_001098101.1:n.1189-4C>G
NM_001165899.1:c.1006-4C>G	NP_001159371.1:n.1006-4C>G
NM_001165899.2:c.1006-4C>G	NP_001159371.1:n.1006-4C>G
NM_001197218.1:c.997-4C>G	NP_001184147.1:n.997-4C>G
NM_001197218.2:c.997-4C>G	NP_001184147.1:n.997-4C>G
NM_001197219.1:c.823-4C>G	NP_001184148.1:n.823-4C>G
NM_001197219.2:c.823-4C>G	NP_001184148.1:n.823-4C>G
NM_001197220.1:c.799-4C>G	NP_001184149.1:n.799-4C>G
NM_001197220.2:c.799-4C>G	NP_001184149.1:n.799-4C>G
NM_001197221.1:c.283-4C>G	NP_001184150.1:n.283-4C>G
NM_001197221.2:c.283-4C>G	NP_001184150.1:n.283-4C>G
NM_001197222.1:c.517-4C>G	NP_001184151.1:n.517-4C>G
NM_001197222.2:c.517-4C>G	NP_001184151.1:n.517-4C>G
NM_001197223.1:c.316-4C>G	NP_001184152.1:n.316-4C>G
NM_001197223.2:c.316-4C>G	NP_001184152.1:n.316-4C>G
NM_001349241.1:c.976-4C>G	NP_001336170.1:n.976-4C>G
NM_001349241.2:c.976-4C>G	NP_001336170.1:n.976-4C>G
NM_001349242.1:c.859-4C>G	NP_001336171.1:n.859-4C>G
NM_001349242.2:c.859-4C>G	NP_001336171.1:n.859-4C>G
NM_001349243.1:c.421-4C>G	NP_001336172.1:n.421-4C>G
NM_001349243.2:c.421-4C>G	NP_001336172.1:n.421-4C>G
NM_001364599.1:c.1006-4C>G	NP_001351528.1:n.1006-4C>G
NM_001364603.1:c.283-4C>G	NP_001351532.1:n.283-4C>G
NM_001364604.1:c.421-4C>G	NP_001351533.1:n.421-4C>G
NM_006203.4:c.781-4C>G	NP_006194.2:n.781-4C>G
NM_006203.5:c.781-4C>G	NP_006194.2:n.781-4C>G
ENST00000309641.10:c.1041-4C>G	ENSP00000308485.6:n.1041-4C>G
ENST00000317118.12:c.316-4C>G	ENSP00000321739.8:n.316-4C>G
ENST00000340635.10:c.1189-4C>G	ENSP00000345502.6:n.1189-4C>G
ENST00000358923.10:c.283-4C>G	ENSP00000351800.6:n.283-4C>G
ENST00000360047.9:c.781-4C>G	ENSP00000353152.5:n.781-4C>G
ENST00000405755.6:c.823-4C>G	ENSP00000384806.2:n.823-4C>G
ENST00000502484.6:c.1006-4C>G	ENSP00000423094.2:n.1006-4C>G
ENST00000503258.5:c.799-4C>G	ENSP00000425605.1:n.799-4C>G
ENST00000505453.1:c.283-4C>G	ENSP00000421013.1:n.283-4C>G
ENST00000507116.5:c.997-4C>G	ENSP00000424852.1:n.997-4C>G
ENST00000507116.6:c.997-4C>G	ENSP00000424852.1:n.997-4C>G
ENST00000515011.5:n.925-4C>G
ENST00000546160.5:c.796-4C>G	ENSP00000442734.2:n.796-4C>G
ENST00000636120.1:c.859-4C>G	ENSP00000490821.1:n.859-4C>G
XM_005248537.2:c.859-4C>G	XP_005248594.1:n.859-4C>G
XM_005248538.3:c.781-4C>G	XP_005248595.1:n.781-4C>G
XM_011543469.1:c.1153-4C>G	XP_011541771.1:n.1153-4C>G
XM_011543470.1:c.1153-4C>G	XP_011541772.1:n.1153-4C>G
XM_011543470.2:c.1153-4C>G	XP_011541772.1:n.1153-4C>G
XM_011543471.1:c.1006-4C>G	XP_011541773.1:n.1006-4C>G
XM_011543471.2:c.1006-4C>G	XP_011541773.1:n.1006-4C>G
XM_011543472.1:c.1006-4C>G	XP_011541774.1:n.1006-4C>G
XM_011543473.1:c.1006-4C>G	XP_011541775.1:n.1006-4C>G
XM_011543474.1:c.976-4C>G	XP_011541776.1:n.976-4C>G
XM_011543475.1:c.823-4C>G	XP_011541777.1:n.823-4C>G
XM_011543476.1:c.769-4C>G	XP_011541778.1:n.769-4C>G
XM_011543477.1:c.748-4C>G	XP_011541779.1:n.748-4C>G
XM_011543478.1:c.685-4C>G	XP_011541780.1:n.685-4C>G
XM_011543479.1:c.685-4C>G	XP_011541781.1:n.685-4C>G
XM_017009565.1:c.1153-4C>G	XP_016865054.1:n.1153-4C>G
XM_017009566.1:c.1006-4C>G	XP_016865055.1:n.1006-4C>G
XM_017009567.1:c.991-4C>G	XP_016865056.1:n.991-4C>G
XM_024446110.1:c.1153-4C>G	XP_024301878.1:n.1153-4C>G
XM_024446112.1:c.1006-4C>G	XP_024301880.1:n.1006-4C>G