Canonical Allele Identifier: CA2673946926

Gene: PDE4D

Linked Data

• gnomAD v4: 5-59193414-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.59193414T>G , CM000667.2:g.59193414T>G	GRCh38
NC_000005.9:g.58489240T>G , CM000667.1:g.58489240T>G	GRCh37
NC_000005.8:g.58524997T>G	NCBI36
NG_027957.1:g.1299686A>C
NG_027957.2:g.1335916A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000507116.6:c.492+86A>C	ENSP00000424852.1:n.492+86A>C
ENST00000340635.11:c.684+86A>C MANE Select	ENSP00000345502.6:n.684+86A>C
ENST00000636120.1:c.354+86A>C	ENSP00000490821.1:n.354+86A>C
ENST00000638939.1:c.249+86A>C	ENSP00000492052.1:n.249+86A>C
ENST00000309641.10:c.492+86A>C	ENSP00000308485.6:n.492+86A>C
ENST00000340635.10:c.684+86A>C	ENSP00000345502.6:n.684+86A>C
ENST00000360047.9:c.276+86A>C	ENSP00000353152.5:n.276+86A>C
ENST00000405053.7:n.347+86A>C
ENST00000405755.6:c.318+86A>C	ENSP00000384806.2:n.318+86A>C
ENST00000502484.6:c.501+86A>C	ENSP00000423094.2:n.501+86A>C
ENST00000502575.1:c.492+86A>C	ENSP00000425917.1:n.492+86A>C
ENST00000503258.5:c.294+86A>C	ENSP00000425605.1:n.294+86A>C
ENST00000505453.1:c.-98-154443A>C	ENSP00000421013.1:n.-98-154443A>C
ENST00000507116.5:c.492+86A>C	ENSP00000424852.1:n.492+86A>C
ENST00000515324.1:n.196+86A>C
ENST00000546160.5:c.291+86A>C	ENSP00000442734.2:n.291+86A>C
ENST00000621323.4:n.229+86A>C
NM_001104631.1:c.684+86A>C	NP_001098101.1:n.684+86A>C
NM_001165899.1:c.501+86A>C	NP_001159371.1:n.501+86A>C
NM_001197218.1:c.492+86A>C	NP_001184147.1:n.492+86A>C
NM_001197219.1:c.318+86A>C	NP_001184148.1:n.318+86A>C
NM_001197220.1:c.294+86A>C	NP_001184149.1:n.294+86A>C
NM_006203.4:c.276+86A>C	NP_006194.2:n.276+86A>C
XM_005248537.2:c.354+86A>C	XP_005248594.1:n.354+86A>C
XM_005248538.3:c.276+86A>C	XP_005248595.1:n.276+86A>C
XM_011543469.1:c.648+86A>C	XP_011541771.1:n.648+86A>C
XM_011543470.1:c.648+86A>C	XP_011541772.1:n.648+86A>C
XM_011543471.1:c.501+86A>C	XP_011541773.1:n.501+86A>C
XM_011543472.1:c.501+86A>C	XP_011541774.1:n.501+86A>C
XM_011543473.1:c.501+86A>C	XP_011541775.1:n.501+86A>C
XM_011543474.1:c.471+86A>C	XP_011541776.1:n.471+86A>C
XM_011543475.1:c.318+86A>C	XP_011541777.1:n.318+86A>C
XM_011543476.1:c.264+86A>C	XP_011541778.1:n.264+86A>C
XM_011543477.1:c.243+86A>C	XP_011541779.1:n.243+86A>C
XM_011543478.1:c.180+86A>C	XP_011541780.1:n.180+86A>C
XM_011543479.1:c.180+86A>C	XP_011541781.1:n.180+86A>C
NM_001349241.1:c.471+86A>C	NP_001336170.1:n.471+86A>C
NM_001349242.1:c.354+86A>C	NP_001336171.1:n.354+86A>C
NM_001349243.1:c.-11+86A>C	NP_001336172.1:n.-11+86A>C
NM_001364599.1:c.501+86A>C	NP_001351528.1:n.501+86A>C
NM_001364600.1:c.501+86A>C	NP_001351529.1:n.501+86A>C
NM_001364602.1:c.492+86A>C	NP_001351531.1:n.492+86A>C
NM_001364603.1:c.-267+86A>C	NP_001351532.1:n.-267+86A>C
NM_001364604.1:c.-11+86A>C	NP_001351533.1:n.-11+86A>C
XM_011543470.2:c.648+86A>C	XP_011541772.1:n.648+86A>C
XM_011543471.2:c.501+86A>C	XP_011541773.1:n.501+86A>C
XM_017009565.1:c.648+86A>C	XP_016865054.1:n.648+86A>C
XM_017009566.1:c.501+86A>C	XP_016865055.1:n.501+86A>C
XM_017009567.1:c.486+86A>C	XP_016865056.1:n.486+86A>C
XM_024446110.1:c.648+86A>C	XP_024301878.1:n.648+86A>C
XM_024446112.1:c.501+86A>C	XP_024301880.1:n.501+86A>C
NM_001104631.2:c.684+86A>C MANE Select	NP_001098101.1:n.684+86A>C
NM_001165899.2:c.501+86A>C	NP_001159371.1:n.501+86A>C
NM_001197218.2:c.492+86A>C	NP_001184147.1:n.492+86A>C
NM_001197219.2:c.318+86A>C	NP_001184148.1:n.318+86A>C
NM_001197220.2:c.294+86A>C	NP_001184149.1:n.294+86A>C
NM_001349241.2:c.471+86A>C	NP_001336170.1:n.471+86A>C
NM_001349243.2:c.-11+86A>C	NP_001336172.1:n.-11+86A>C
NM_001364600.2:c.501+86A>C	NP_001351529.1:n.501+86A>C
NM_001364602.2:c.492+86A>C	NP_001351531.1:n.492+86A>C
NM_001349242.2:c.354+86A>C	NP_001336171.1:n.354+86A>C
NM_006203.5:c.276+86A>C	NP_006194.2:n.276+86A>C