Canonical Allele Identifier: CA812602521

Gene: PDE4D

Linked Data

• dbSNP Id: rs1838720
• MyVariant Identifiers: chr5:g.58599389T>G (hg19) ; chr5:g.59303563T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.59303563T>G , CM000667.2:g.59303563T>G	GRCh38
NC_000005.9:g.58599389T>G , CM000667.1:g.58599389T>G	GRCh37
NC_000005.8:g.58635146T>G	NCBI36
NG_027957.1:g.1189537A>C
NG_027957.2:g.1225767A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000507116.6:c.264-87595A>C	ENSP00000424852.1:n.264-87595A>C
ENST00000340635.11:c.456-87595A>C MANE Select	ENSP00000345502.6:n.456-87595A>C
ENST00000636120.1:c.126-87595A>C	ENSP00000490821.1:n.126-87595A>C
ENST00000309641.10:c.264-87595A>C	ENSP00000308485.6:n.264-87595A>C
ENST00000340635.10:c.456-87595A>C	ENSP00000345502.6:n.456-87595A>C
ENST00000360047.9:c.48-87595A>C	ENSP00000353152.5:n.48-87595A>C
ENST00000405053.7:n.119-87595A>C
ENST00000405755.6:c.89+53195A>C	ENSP00000384806.2:n.89+53195A>C
ENST00000502484.6:c.273-87595A>C	ENSP00000423094.2:n.273-87595A>C
ENST00000502575.1:c.264-87595A>C	ENSP00000425917.1:n.264-87595A>C
ENST00000505453.1:c.-98-264592A>C	ENSP00000421013.1:n.-98-264592A>C
ENST00000507116.5:c.264-87595A>C	ENSP00000424852.1:n.264-87595A>C
ENST00000514231.1:n.219-87595A>C
NM_001104631.1:c.456-87595A>C	NP_001098101.1:n.456-87595A>C
NM_001165899.1:c.273-87595A>C	NP_001159371.1:n.273-87595A>C
NM_001197218.1:c.264-87595A>C	NP_001184147.1:n.264-87595A>C
NM_001197219.1:c.89+53195A>C	NP_001184148.1:n.89+53195A>C
NM_006203.4:c.48-87595A>C	NP_006194.2:n.48-87595A>C
XM_005248537.2:c.126-87595A>C	XP_005248594.1:n.126-87595A>C
XM_005248538.3:c.48-87595A>C	XP_005248595.1:n.48-87595A>C
XM_011543469.1:c.420-87595A>C	XP_011541771.1:n.420-87595A>C
XM_011543470.1:c.420-87595A>C	XP_011541772.1:n.420-87595A>C
XM_011543471.1:c.273-87595A>C	XP_011541773.1:n.273-87595A>C
XM_011543472.1:c.273-87595A>C	XP_011541774.1:n.273-87595A>C
XM_011543473.1:c.273-87595A>C	XP_011541775.1:n.273-87595A>C
XM_011543474.1:c.243-87595A>C	XP_011541776.1:n.243-87595A>C
XM_011543475.1:c.90-87595A>C	XP_011541777.1:n.90-87595A>C
XM_011543476.1:c.36-87595A>C	XP_011541778.1:n.36-87595A>C
XM_011543477.1:c.15-87595A>C	XP_011541779.1:n.15-87595A>C
XM_011543478.1:c.-50+79207A>C	XP_011541780.1:n.-50+79207A>C
NM_001349241.1:c.243-87595A>C	NP_001336170.1:n.243-87595A>C
NM_001349242.1:c.126-87595A>C	NP_001336171.1:n.126-87595A>C
NM_001349243.1:c.-239-87595A>C	NP_001336172.1:n.-239-87595A>C
NM_001364599.1:c.273-87595A>C	NP_001351528.1:n.273-87595A>C
NM_001364600.1:c.273-87595A>C	NP_001351529.1:n.273-87595A>C
NM_001364601.1:c.264-87595A>C	NP_001351530.1:n.264-87595A>C
NM_001364602.1:c.264-87595A>C	NP_001351531.1:n.264-87595A>C
NM_001364603.1:c.-495-87595A>C	NP_001351532.1:n.-495-87595A>C
NM_001364604.1:c.-239-87595A>C	NP_001351533.1:n.-239-87595A>C
XM_011543470.2:c.420-87595A>C	XP_011541772.1:n.420-87595A>C
XM_011543471.2:c.273-87595A>C	XP_011541773.1:n.273-87595A>C
XM_017009565.1:c.420-87595A>C	XP_016865054.1:n.420-87595A>C
XM_017009566.1:c.273-87595A>C	XP_016865055.1:n.273-87595A>C
XM_017009567.1:c.258-87595A>C	XP_016865056.1:n.258-87595A>C
XM_024446110.1:c.420-87595A>C	XP_024301878.1:n.420-87595A>C
XM_024446112.1:c.273-87595A>C	XP_024301880.1:n.273-87595A>C
NM_001104631.2:c.456-87595A>C MANE Select	NP_001098101.1:n.456-87595A>C
NM_001165899.2:c.273-87595A>C	NP_001159371.1:n.273-87595A>C
NM_001197218.2:c.264-87595A>C	NP_001184147.1:n.264-87595A>C
NM_001197219.2:c.89+53195A>C	NP_001184148.1:n.89+53195A>C
NM_001349241.2:c.243-87595A>C	NP_001336170.1:n.243-87595A>C
NM_001349243.2:c.-239-87595A>C	NP_001336172.1:n.-239-87595A>C
NM_001364600.2:c.273-87595A>C	NP_001351529.1:n.273-87595A>C
NM_001364602.2:c.264-87595A>C	NP_001351531.1:n.264-87595A>C
NM_001349242.2:c.126-87595A>C	NP_001336171.1:n.126-87595A>C
NM_006203.5:c.48-87595A>C	NP_006194.2:n.48-87595A>C