Canonical Allele Identifier: CA359930611

Gene: PDE4D

Linked Data

• MyVariant Identifiers: chr5:g.58511605A>C (hg19) ; chr5:g.59215779A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.59215779A>C , CM000667.2:g.59215779A>C	GRCh38
NC_000005.9:g.58511605A>C , CM000667.1:g.58511605A>C	GRCh37
NC_000005.8:g.58547362A>C	NCBI36
NG_027957.1:g.1277321T>G
NG_027957.2:g.1313551T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507116.6:c.453T>G	ENSP00000424852.1:p.Asp151Glu
ENST00000340635.11:c.645T>G MANE Select	ENSP00000345502.6:p.Asp215Glu
ENST00000636120.1:c.315T>G	ENSP00000490821.1:p.Asp105Glu
ENST00000638939.1:c.210T>G	ENSP00000492052.1:p.Asp70Glu
ENST00000309641.10:c.453T>G	ENSP00000308485.6:p.Asp151Glu
ENST00000340635.10:c.645T>G	ENSP00000345502.6:p.Asp215Glu
ENST00000360047.9:c.237T>G	ENSP00000353152.5:p.Asp79Glu
ENST00000405053.7:n.308T>G
ENST00000405755.6:c.279T>G	ENSP00000384806.2:p.Asp93Glu
ENST00000502484.6:c.462T>G	ENSP00000423094.2:p.Asp154Glu
ENST00000502575.1:c.453T>G	ENSP00000425917.1:p.Asp151Glu
ENST00000503258.5:c.255T>G	ENSP00000425605.1:p.Asp85Glu
ENST00000505453.1:c.-98-176808T>G	ENSP00000421013.1:n.-98-176808T>G
ENST00000507116.5:c.453T>G	ENSP00000424852.1:p.Asp151Glu
ENST00000514231.1:n.408T>G
ENST00000515324.1:n.157T>G
ENST00000546160.5:c.252T>G	ENSP00000442734.2:p.Asp84Glu
ENST00000621323.4:n.190T>G
NM_001104631.1:c.645T>G	NP_001098101.1:p.Asp215Glu
NM_001165899.1:c.462T>G	NP_001159371.1:p.Asp154Glu
NM_001197218.1:c.453T>G	NP_001184147.1:p.Asp151Glu
NM_001197219.1:c.279T>G	NP_001184148.1:p.Asp93Glu
NM_001197220.1:c.255T>G	NP_001184149.1:p.Asp85Glu
NM_006203.4:c.237T>G	NP_006194.2:p.Asp79Glu
XM_005248537.2:c.315T>G	XP_005248594.1:p.Asp105Glu
XM_005248538.3:c.237T>G	XP_005248595.1:p.Asp79Glu
XM_011543469.1:c.609T>G	XP_011541771.1:p.Asp203Glu
XM_011543470.1:c.609T>G	XP_011541772.1:p.Asp203Glu
XM_011543471.1:c.462T>G	XP_011541773.1:p.Asp154Glu
XM_011543472.1:c.462T>G	XP_011541774.1:p.Asp154Glu
XM_011543473.1:c.462T>G	XP_011541775.1:p.Asp154Glu
XM_011543474.1:c.432T>G	XP_011541776.1:p.Asp144Glu
XM_011543475.1:c.279T>G	XP_011541777.1:p.Asp93Glu
XM_011543476.1:c.225T>G	XP_011541778.1:p.Asp75Glu
XM_011543477.1:c.204T>G	XP_011541779.1:p.Asp68Glu
XM_011543478.1:c.141T>G	XP_011541780.1:p.Asp47Glu
XM_011543479.1:c.141T>G	XP_011541781.1:p.Asp47Glu
NM_001349241.1:c.432T>G	NP_001336170.1:p.Asp144Glu
NM_001349242.1:c.315T>G	NP_001336171.1:p.Asp105Glu
NM_001349243.1:c.-50T>G	NP_001336172.1:n.-50T>G
NM_001364599.1:c.462T>G	NP_001351528.1:p.Asp154Glu
NM_001364600.1:c.462T>G	NP_001351529.1:p.Asp154Glu
NM_001364601.1:c.453T>G	NP_001351530.1:p.Asp151Glu
NM_001364602.1:c.453T>G	NP_001351531.1:p.Asp151Glu
NM_001364603.1:c.-306T>G	NP_001351532.1:n.-306T>G
NM_001364604.1:c.-50T>G	NP_001351533.1:n.-50T>G
XM_011543470.2:c.609T>G	XP_011541772.1:p.Asp203Glu
XM_011543471.2:c.462T>G	XP_011541773.1:p.Asp154Glu
XM_017009565.1:c.609T>G	XP_016865054.1:p.Asp203Glu
XM_017009566.1:c.462T>G	XP_016865055.1:p.Asp154Glu
XM_017009567.1:c.447T>G	XP_016865056.1:p.Asp149Glu
XM_024446110.1:c.609T>G	XP_024301878.1:p.Asp203Glu
XM_024446112.1:c.462T>G	XP_024301880.1:p.Asp154Glu
NM_001104631.2:c.645T>G MANE Select	NP_001098101.1:p.Asp215Glu
NM_001165899.2:c.462T>G	NP_001159371.1:p.Asp154Glu
NM_001197218.2:c.453T>G	NP_001184147.1:p.Asp151Glu
NM_001197219.2:c.279T>G	NP_001184148.1:p.Asp93Glu
NM_001197220.2:c.255T>G	NP_001184149.1:p.Asp85Glu
NM_001349241.2:c.432T>G	NP_001336170.1:p.Asp144Glu
NM_001349243.2:c.-50T>G	NP_001336172.1:n.-50T>G
NM_001364600.2:c.462T>G	NP_001351529.1:p.Asp154Glu
NM_001364602.2:c.453T>G	NP_001351531.1:p.Asp151Glu
NM_001349242.2:c.315T>G	NP_001336171.1:p.Asp105Glu
NM_006203.5:c.237T>G	NP_006194.2:p.Asp79Glu