Canonical Allele Identifier: CA359930920

Gene: PDE4D

Linked Data

• MyVariant Identifiers: chr5:g.58511696C>A (hg19) ; chr5:g.59215870C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.59215870C>A , CM000667.2:g.59215870C>A	GRCh38
NC_000005.9:g.58511696C>A , CM000667.1:g.58511696C>A	GRCh37
NC_000005.8:g.58547453C>A	NCBI36
NG_027957.1:g.1277230G>T
NG_027957.2:g.1313460G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507116.6:c.362G>T	ENSP00000424852.1:p.Ser121Ile
ENST00000340635.11:c.554G>T MANE Select	ENSP00000345502.6:p.Ser185Ile
ENST00000636120.1:c.224G>T	ENSP00000490821.1:p.Ser75Ile
ENST00000638939.1:c.119G>T	ENSP00000492052.1:p.Ser40Ile
ENST00000309641.10:c.362G>T	ENSP00000308485.6:p.Ser121Ile
ENST00000340635.10:c.554G>T	ENSP00000345502.6:p.Ser185Ile
ENST00000360047.9:c.146G>T	ENSP00000353152.5:p.Ser49Ile
ENST00000405053.7:n.217G>T
ENST00000405755.6:c.188G>T	ENSP00000384806.2:p.Ser63Ile
ENST00000502484.6:c.371G>T	ENSP00000423094.2:p.Ser124Ile
ENST00000502575.1:c.362G>T	ENSP00000425917.1:p.Ser121Ile
ENST00000503258.5:c.164G>T	ENSP00000425605.1:p.Ser55Ile
ENST00000505453.1:c.-98-176899G>T	ENSP00000421013.1:n.-98-176899G>T
ENST00000507116.5:c.362G>T	ENSP00000424852.1:p.Ser121Ile
ENST00000514231.1:n.317G>T
ENST00000515324.1:n.66G>T
ENST00000546160.5:c.161G>T	ENSP00000442734.2:p.Ser54Ile
ENST00000621323.4:n.99G>T
NM_001104631.1:c.554G>T	NP_001098101.1:p.Ser185Ile
NM_001165899.1:c.371G>T	NP_001159371.1:p.Ser124Ile
NM_001197218.1:c.362G>T	NP_001184147.1:p.Ser121Ile
NM_001197219.1:c.188G>T	NP_001184148.1:p.Ser63Ile
NM_001197220.1:c.164G>T	NP_001184149.1:p.Ser55Ile
NM_006203.4:c.146G>T	NP_006194.2:p.Ser49Ile
XM_005248537.2:c.224G>T	XP_005248594.1:p.Ser75Ile
XM_005248538.3:c.146G>T	XP_005248595.1:p.Ser49Ile
XM_011543469.1:c.518G>T	XP_011541771.1:p.Ser173Ile
XM_011543470.1:c.518G>T	XP_011541772.1:p.Ser173Ile
XM_011543471.1:c.371G>T	XP_011541773.1:p.Ser124Ile
XM_011543472.1:c.371G>T	XP_011541774.1:p.Ser124Ile
XM_011543473.1:c.371G>T	XP_011541775.1:p.Ser124Ile
XM_011543474.1:c.341G>T	XP_011541776.1:p.Ser114Ile
XM_011543475.1:c.188G>T	XP_011541777.1:p.Ser63Ile
XM_011543476.1:c.134G>T	XP_011541778.1:p.Ser45Ile
XM_011543477.1:c.113G>T	XP_011541779.1:p.Ser38Ile
XM_011543478.1:c.50G>T	XP_011541780.1:p.Ser17Ile
XM_011543479.1:c.50G>T	XP_011541781.1:p.Ser17Ile
NM_001349241.1:c.341G>T	NP_001336170.1:p.Ser114Ile
NM_001349242.1:c.224G>T	NP_001336171.1:p.Ser75Ile
NM_001349243.1:c.-141G>T	NP_001336172.1:n.-141G>T
NM_001364599.1:c.371G>T	NP_001351528.1:p.Ser124Ile
NM_001364600.1:c.371G>T	NP_001351529.1:p.Ser124Ile
NM_001364601.1:c.362G>T	NP_001351530.1:p.Ser121Ile
NM_001364602.1:c.362G>T	NP_001351531.1:p.Ser121Ile
NM_001364603.1:c.-397G>T	NP_001351532.1:n.-397G>T
NM_001364604.1:c.-141G>T	NP_001351533.1:n.-141G>T
XM_011543470.2:c.518G>T	XP_011541772.1:p.Ser173Ile
XM_011543471.2:c.371G>T	XP_011541773.1:p.Ser124Ile
XM_017009565.1:c.518G>T	XP_016865054.1:p.Ser173Ile
XM_017009566.1:c.371G>T	XP_016865055.1:p.Ser124Ile
XM_017009567.1:c.356G>T	XP_016865056.1:p.Ser119Ile
XM_024446110.1:c.518G>T	XP_024301878.1:p.Ser173Ile
XM_024446112.1:c.371G>T	XP_024301880.1:p.Ser124Ile
NM_001104631.2:c.554G>T MANE Select	NP_001098101.1:p.Ser185Ile
NM_001165899.2:c.371G>T	NP_001159371.1:p.Ser124Ile
NM_001197218.2:c.362G>T	NP_001184147.1:p.Ser121Ile
NM_001197219.2:c.188G>T	NP_001184148.1:p.Ser63Ile
NM_001197220.2:c.164G>T	NP_001184149.1:p.Ser55Ile
NM_001349241.2:c.341G>T	NP_001336170.1:p.Ser114Ile
NM_001349243.2:c.-141G>T	NP_001336172.1:n.-141G>T
NM_001364600.2:c.371G>T	NP_001351529.1:p.Ser124Ile
NM_001364602.2:c.362G>T	NP_001351531.1:p.Ser121Ile
NM_001349242.2:c.224G>T	NP_001336171.1:p.Ser75Ile
NM_006203.5:c.146G>T	NP_006194.2:p.Ser49Ile