Canonical Allele Identifier: CA359930900

Gene: PDE4D

Linked Data

• COSMIC: COSM4921837 ; COSM4921838 ; COSM4921839 ; COSM4921840 ; COSM4921841 ; COSM4921842 ; COSM4921843
• MyVariant Identifiers: chr5:g.58511685C>A (hg19) ; chr5:g.59215859C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.59215859C>A , CM000667.2:g.59215859C>A	GRCh38
NC_000005.9:g.58511685C>A , CM000667.1:g.58511685C>A	GRCh37
NC_000005.8:g.58547442C>A	NCBI36
NG_027957.1:g.1277241G>T
NG_027957.2:g.1313471G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000507116.6:c.373G>T	ENSP00000424852.1:p.Glu125Ter
ENST00000340635.11:c.565G>T MANE Select	ENSP00000345502.6:p.Glu189Ter
ENST00000636120.1:c.235G>T	ENSP00000490821.1:p.Glu79Ter
ENST00000638939.1:c.130G>T	ENSP00000492052.1:p.Glu44Ter
ENST00000309641.10:c.373G>T	ENSP00000308485.6:p.Glu125Ter
ENST00000340635.10:c.565G>T	ENSP00000345502.6:p.Glu189Ter
ENST00000360047.9:c.157G>T	ENSP00000353152.5:p.Glu53Ter
ENST00000405053.7:n.228G>T
ENST00000405755.6:c.199G>T	ENSP00000384806.2:p.Glu67Ter
ENST00000502484.6:c.382G>T	ENSP00000423094.2:p.Glu128Ter
ENST00000502575.1:c.373G>T	ENSP00000425917.1:p.Glu125Ter
ENST00000503258.5:c.175G>T	ENSP00000425605.1:p.Glu59Ter
ENST00000505453.1:c.-98-176888G>T	ENSP00000421013.1:n.-98-176888G>T
ENST00000507116.5:c.373G>T	ENSP00000424852.1:p.Glu125Ter
ENST00000514231.1:n.328G>T
ENST00000515324.1:n.77G>T
ENST00000546160.5:c.172G>T	ENSP00000442734.2:p.Glu58Ter
ENST00000621323.4:n.110G>T
NM_001104631.1:c.565G>T	NP_001098101.1:p.Glu189Ter
NM_001165899.1:c.382G>T	NP_001159371.1:p.Glu128Ter
NM_001197218.1:c.373G>T	NP_001184147.1:p.Glu125Ter
NM_001197219.1:c.199G>T	NP_001184148.1:p.Glu67Ter
NM_001197220.1:c.175G>T	NP_001184149.1:p.Glu59Ter
NM_006203.4:c.157G>T	NP_006194.2:p.Glu53Ter
XM_005248537.2:c.235G>T	XP_005248594.1:p.Glu79Ter
XM_005248538.3:c.157G>T	XP_005248595.1:p.Glu53Ter
XM_011543469.1:c.529G>T	XP_011541771.1:p.Glu177Ter
XM_011543470.1:c.529G>T	XP_011541772.1:p.Glu177Ter
XM_011543471.1:c.382G>T	XP_011541773.1:p.Glu128Ter
XM_011543472.1:c.382G>T	XP_011541774.1:p.Glu128Ter
XM_011543473.1:c.382G>T	XP_011541775.1:p.Glu128Ter
XM_011543474.1:c.352G>T	XP_011541776.1:p.Glu118Ter
XM_011543475.1:c.199G>T	XP_011541777.1:p.Glu67Ter
XM_011543476.1:c.145G>T	XP_011541778.1:p.Glu49Ter
XM_011543477.1:c.124G>T	XP_011541779.1:p.Glu42Ter
XM_011543478.1:c.61G>T	XP_011541780.1:p.Glu21Ter
XM_011543479.1:c.61G>T	XP_011541781.1:p.Glu21Ter
NM_001349241.1:c.352G>T	NP_001336170.1:p.Glu118Ter
NM_001349242.1:c.235G>T	NP_001336171.1:p.Glu79Ter
NM_001349243.1:c.-130G>T	NP_001336172.1:n.-130G>T
NM_001364599.1:c.382G>T	NP_001351528.1:p.Glu128Ter
NM_001364600.1:c.382G>T	NP_001351529.1:p.Glu128Ter
NM_001364601.1:c.373G>T	NP_001351530.1:p.Glu125Ter
NM_001364602.1:c.373G>T	NP_001351531.1:p.Glu125Ter
NM_001364603.1:c.-386G>T	NP_001351532.1:n.-386G>T
NM_001364604.1:c.-130G>T	NP_001351533.1:n.-130G>T
XM_011543470.2:c.529G>T	XP_011541772.1:p.Glu177Ter
XM_011543471.2:c.382G>T	XP_011541773.1:p.Glu128Ter
XM_017009565.1:c.529G>T	XP_016865054.1:p.Glu177Ter
XM_017009566.1:c.382G>T	XP_016865055.1:p.Glu128Ter
XM_017009567.1:c.367G>T	XP_016865056.1:p.Glu123Ter
XM_024446110.1:c.529G>T	XP_024301878.1:p.Glu177Ter
XM_024446112.1:c.382G>T	XP_024301880.1:p.Glu128Ter
NM_001104631.2:c.565G>T MANE Select	NP_001098101.1:p.Glu189Ter
NM_001165899.2:c.382G>T	NP_001159371.1:p.Glu128Ter
NM_001197218.2:c.373G>T	NP_001184147.1:p.Glu125Ter
NM_001197219.2:c.199G>T	NP_001184148.1:p.Glu67Ter
NM_001197220.2:c.175G>T	NP_001184149.1:p.Glu59Ter
NM_001349241.2:c.352G>T	NP_001336170.1:p.Glu118Ter
NM_001349243.2:c.-130G>T	NP_001336172.1:n.-130G>T
NM_001364600.2:c.382G>T	NP_001351529.1:p.Glu128Ter
NM_001364602.2:c.373G>T	NP_001351531.1:p.Glu125Ter
NM_001349242.2:c.235G>T	NP_001336171.1:p.Glu79Ter
NM_006203.5:c.157G>T	NP_006194.2:p.Glu53Ter