Canonical Allele Identifier: CA444501338

Gene: PDE4D

Linked Data

• gnomAD v4: 5-59215854-G-A
• COSMIC: COSM4500664 ; COSM4500665 ; COSM4500666 ; COSM4500667 ; COSM4500668 ; COSM4500669 ; COSM4500670
• MyVariant Identifiers: chr5:g.58511680G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.59215854G>A , CM000667.2:g.59215854G>A	GRCh38
NC_000005.9:g.58511680G>A , CM000667.1:g.58511680G>A	GRCh37
NC_000005.8:g.58547437G>A	NCBI36
NG_027957.1:g.1277246C>T
NG_027957.2:g.1313476C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507116.6:c.378C>T	ENSP00000424852.1:p.Ser126=
ENST00000340635.11:c.570C>T MANE Select	ENSP00000345502.6:p.Ser190=
ENST00000636120.1:c.240C>T	ENSP00000490821.1:p.Ser80=
ENST00000638939.1:c.135C>T	ENSP00000492052.1:p.Ser45=
ENST00000309641.10:c.378C>T	ENSP00000308485.6:p.Ser126=
ENST00000340635.10:c.570C>T	ENSP00000345502.6:p.Ser190=
ENST00000360047.9:c.162C>T	ENSP00000353152.5:p.Ser54=
ENST00000405053.7:n.233C>T
ENST00000405755.6:c.204C>T	ENSP00000384806.2:p.Ser68=
ENST00000502484.6:c.387C>T	ENSP00000423094.2:p.Ser129=
ENST00000502575.1:c.378C>T	ENSP00000425917.1:p.Ser126=
ENST00000503258.5:c.180C>T	ENSP00000425605.1:p.Ser60=
ENST00000505453.1:c.-98-176883C>T	ENSP00000421013.1:n.-98-176883C>T
ENST00000507116.5:c.378C>T	ENSP00000424852.1:p.Ser126=
ENST00000514231.1:n.333C>T
ENST00000515324.1:n.82C>T
ENST00000546160.5:c.177C>T	ENSP00000442734.2:p.Ser59=
ENST00000621323.4:n.115C>T
NM_001104631.1:c.570C>T	NP_001098101.1:p.Ser190=
NM_001165899.1:c.387C>T	NP_001159371.1:p.Ser129=
NM_001197218.1:c.378C>T	NP_001184147.1:p.Ser126=
NM_001197219.1:c.204C>T	NP_001184148.1:p.Ser68=
NM_001197220.1:c.180C>T	NP_001184149.1:p.Ser60=
NM_006203.4:c.162C>T	NP_006194.2:p.Ser54=
XM_005248537.2:c.240C>T	XP_005248594.1:p.Ser80=
XM_005248538.3:c.162C>T	XP_005248595.1:p.Ser54=
XM_011543469.1:c.534C>T	XP_011541771.1:p.Ser178=
XM_011543470.1:c.534C>T	XP_011541772.1:p.Ser178=
XM_011543471.1:c.387C>T	XP_011541773.1:p.Ser129=
XM_011543472.1:c.387C>T	XP_011541774.1:p.Ser129=
XM_011543473.1:c.387C>T	XP_011541775.1:p.Ser129=
XM_011543474.1:c.357C>T	XP_011541776.1:p.Ser119=
XM_011543475.1:c.204C>T	XP_011541777.1:p.Ser68=
XM_011543476.1:c.150C>T	XP_011541778.1:p.Ser50=
XM_011543477.1:c.129C>T	XP_011541779.1:p.Ser43=
XM_011543478.1:c.66C>T	XP_011541780.1:p.Ser22=
XM_011543479.1:c.66C>T	XP_011541781.1:p.Ser22=
NM_001349241.1:c.357C>T	NP_001336170.1:p.Ser119=
NM_001349242.1:c.240C>T	NP_001336171.1:p.Ser80=
NM_001349243.1:c.-125C>T	NP_001336172.1:n.-125C>T
NM_001364599.1:c.387C>T	NP_001351528.1:p.Ser129=
NM_001364600.1:c.387C>T	NP_001351529.1:p.Ser129=
NM_001364601.1:c.378C>T	NP_001351530.1:p.Ser126=
NM_001364602.1:c.378C>T	NP_001351531.1:p.Ser126=
NM_001364603.1:c.-381C>T	NP_001351532.1:n.-381C>T
NM_001364604.1:c.-125C>T	NP_001351533.1:n.-125C>T
XM_011543470.2:c.534C>T	XP_011541772.1:p.Ser178=
XM_011543471.2:c.387C>T	XP_011541773.1:p.Ser129=
XM_017009565.1:c.534C>T	XP_016865054.1:p.Ser178=
XM_017009566.1:c.387C>T	XP_016865055.1:p.Ser129=
XM_017009567.1:c.372C>T	XP_016865056.1:p.Ser124=
XM_024446110.1:c.534C>T	XP_024301878.1:p.Ser178=
XM_024446112.1:c.387C>T	XP_024301880.1:p.Ser129=
NM_001104631.2:c.570C>T MANE Select	NP_001098101.1:p.Ser190=
NM_001165899.2:c.387C>T	NP_001159371.1:p.Ser129=
NM_001197218.2:c.378C>T	NP_001184147.1:p.Ser126=
NM_001197219.2:c.204C>T	NP_001184148.1:p.Ser68=
NM_001197220.2:c.180C>T	NP_001184149.1:p.Ser60=
NM_001349241.2:c.357C>T	NP_001336170.1:p.Ser119=
NM_001349243.2:c.-125C>T	NP_001336172.1:n.-125C>T
NM_001364600.2:c.387C>T	NP_001351529.1:p.Ser129=
NM_001364602.2:c.378C>T	NP_001351531.1:p.Ser126=
NM_001349242.2:c.240C>T	NP_001336171.1:p.Ser80=
NM_006203.5:c.162C>T	NP_006194.2:p.Ser54=