Canonical Allele Identifier: CA359930479

Gene: PDE4D

Linked Data

• MyVariant Identifiers: chr5:g.58489331C>A (hg19) ; chr5:g.59193505C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.59193505C>A , CM000667.2:g.59193505C>A	GRCh38
NC_000005.9:g.58489331C>A , CM000667.1:g.58489331C>A	GRCh37
NC_000005.8:g.58525088C>A	NCBI36
NG_027957.1:g.1299595G>T
NG_027957.2:g.1335825G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507116.6:c.487G>T	ENSP00000424852.1:p.Ala163Ser
ENST00000340635.11:c.679G>T MANE Select	ENSP00000345502.6:p.Ala227Ser
ENST00000636120.1:c.349G>T	ENSP00000490821.1:p.Ala117Ser
ENST00000638939.1:c.244G>T	ENSP00000492052.1:p.Ala82Ser
ENST00000309641.10:c.487G>T	ENSP00000308485.6:p.Ala163Ser
ENST00000340635.10:c.679G>T	ENSP00000345502.6:p.Ala227Ser
ENST00000360047.9:c.271G>T	ENSP00000353152.5:p.Ala91Ser
ENST00000405053.7:n.342G>T
ENST00000405755.6:c.313G>T	ENSP00000384806.2:p.Ala105Ser
ENST00000502484.6:c.496G>T	ENSP00000423094.2:p.Ala166Ser
ENST00000502575.1:c.487G>T	ENSP00000425917.1:p.Ala163Ser
ENST00000503258.5:c.289G>T	ENSP00000425605.1:p.Ala97Ser
ENST00000505453.1:c.-98-154534G>T	ENSP00000421013.1:n.-98-154534G>T
ENST00000507116.5:c.487G>T	ENSP00000424852.1:p.Ala163Ser
ENST00000515324.1:n.191G>T
ENST00000546160.5:c.286G>T	ENSP00000442734.2:p.Ala96Ser
ENST00000621323.4:n.224G>T
NM_001104631.1:c.679G>T	NP_001098101.1:p.Ala227Ser
NM_001165899.1:c.496G>T	NP_001159371.1:p.Ala166Ser
NM_001197218.1:c.487G>T	NP_001184147.1:p.Ala163Ser
NM_001197219.1:c.313G>T	NP_001184148.1:p.Ala105Ser
NM_001197220.1:c.289G>T	NP_001184149.1:p.Ala97Ser
NM_006203.4:c.271G>T	NP_006194.2:p.Ala91Ser
XM_005248537.2:c.349G>T	XP_005248594.1:p.Ala117Ser
XM_005248538.3:c.271G>T	XP_005248595.1:p.Ala91Ser
XM_011543469.1:c.643G>T	XP_011541771.1:p.Ala215Ser
XM_011543470.1:c.643G>T	XP_011541772.1:p.Ala215Ser
XM_011543471.1:c.496G>T	XP_011541773.1:p.Ala166Ser
XM_011543472.1:c.496G>T	XP_011541774.1:p.Ala166Ser
XM_011543473.1:c.496G>T	XP_011541775.1:p.Ala166Ser
XM_011543474.1:c.466G>T	XP_011541776.1:p.Ala156Ser
XM_011543475.1:c.313G>T	XP_011541777.1:p.Ala105Ser
XM_011543476.1:c.259G>T	XP_011541778.1:p.Ala87Ser
XM_011543477.1:c.238G>T	XP_011541779.1:p.Ala80Ser
XM_011543478.1:c.175G>T	XP_011541780.1:p.Ala59Ser
XM_011543479.1:c.175G>T	XP_011541781.1:p.Ala59Ser
NM_001349241.1:c.466G>T	NP_001336170.1:p.Ala156Ser
NM_001349242.1:c.349G>T	NP_001336171.1:p.Ala117Ser
NM_001349243.1:c.-16G>T	NP_001336172.1:n.-16G>T
NM_001364599.1:c.496G>T	NP_001351528.1:p.Ala166Ser
NM_001364600.1:c.496G>T	NP_001351529.1:p.Ala166Ser
NM_001364602.1:c.487G>T	NP_001351531.1:p.Ala163Ser
NM_001364603.1:c.-272G>T	NP_001351532.1:n.-272G>T
NM_001364604.1:c.-16G>T	NP_001351533.1:n.-16G>T
XM_011543470.2:c.643G>T	XP_011541772.1:p.Ala215Ser
XM_011543471.2:c.496G>T	XP_011541773.1:p.Ala166Ser
XM_017009565.1:c.643G>T	XP_016865054.1:p.Ala215Ser
XM_017009566.1:c.496G>T	XP_016865055.1:p.Ala166Ser
XM_017009567.1:c.481G>T	XP_016865056.1:p.Ala161Ser
XM_024446110.1:c.643G>T	XP_024301878.1:p.Ala215Ser
XM_024446112.1:c.496G>T	XP_024301880.1:p.Ala166Ser
NM_001104631.2:c.679G>T MANE Select	NP_001098101.1:p.Ala227Ser
NM_001165899.2:c.496G>T	NP_001159371.1:p.Ala166Ser
NM_001197218.2:c.487G>T	NP_001184147.1:p.Ala163Ser
NM_001197219.2:c.313G>T	NP_001184148.1:p.Ala105Ser
NM_001197220.2:c.289G>T	NP_001184149.1:p.Ala97Ser
NM_001349241.2:c.466G>T	NP_001336170.1:p.Ala156Ser
NM_001349243.2:c.-16G>T	NP_001336172.1:n.-16G>T
NM_001364600.2:c.496G>T	NP_001351529.1:p.Ala166Ser
NM_001364602.2:c.487G>T	NP_001351531.1:p.Ala163Ser
NM_001349242.2:c.349G>T	NP_001336171.1:p.Ala117Ser
NM_006203.5:c.271G>T	NP_006194.2:p.Ala91Ser