Canonical Allele Identifier: CA444501206

Gene: PDE4D

Linked Data

• MyVariant Identifiers: chr5:g.58489362T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.59193536T>A , CM000667.2:g.59193536T>A	GRCh38
NC_000005.9:g.58489362T>A , CM000667.1:g.58489362T>A	GRCh37
NC_000005.8:g.58525119T>A	NCBI36
NG_027957.1:g.1299564A>T
NG_027957.2:g.1335794A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507116.6:c.456A>T	ENSP00000424852.1:p.Ile152=
ENST00000340635.11:c.648A>T MANE Select	ENSP00000345502.6:p.Ile216=
ENST00000636120.1:c.318A>T	ENSP00000490821.1:p.Ile106=
ENST00000638939.1:c.213A>T	ENSP00000492052.1:p.Ile71=
ENST00000309641.10:c.456A>T	ENSP00000308485.6:p.Ile152=
ENST00000340635.10:c.648A>T	ENSP00000345502.6:p.Ile216=
ENST00000360047.9:c.240A>T	ENSP00000353152.5:p.Ile80=
ENST00000405053.7:n.311A>T
ENST00000405755.6:c.282A>T	ENSP00000384806.2:p.Ile94=
ENST00000502484.6:c.465A>T	ENSP00000423094.2:p.Ile155=
ENST00000502575.1:c.456A>T	ENSP00000425917.1:p.Ile152=
ENST00000503258.5:c.258A>T	ENSP00000425605.1:p.Ile86=
ENST00000505453.1:c.-98-154565A>T	ENSP00000421013.1:n.-98-154565A>T
ENST00000507116.5:c.456A>T	ENSP00000424852.1:p.Ile152=
ENST00000515324.1:n.160A>T
ENST00000546160.5:c.255A>T	ENSP00000442734.2:p.Ile85=
ENST00000621323.4:n.193A>T
NM_001104631.1:c.648A>T	NP_001098101.1:p.Ile216=
NM_001165899.1:c.465A>T	NP_001159371.1:p.Ile155=
NM_001197218.1:c.456A>T	NP_001184147.1:p.Ile152=
NM_001197219.1:c.282A>T	NP_001184148.1:p.Ile94=
NM_001197220.1:c.258A>T	NP_001184149.1:p.Ile86=
NM_006203.4:c.240A>T	NP_006194.2:p.Ile80=
XM_005248537.2:c.318A>T	XP_005248594.1:p.Ile106=
XM_005248538.3:c.240A>T	XP_005248595.1:p.Ile80=
XM_011543469.1:c.612A>T	XP_011541771.1:p.Ile204=
XM_011543470.1:c.612A>T	XP_011541772.1:p.Ile204=
XM_011543471.1:c.465A>T	XP_011541773.1:p.Ile155=
XM_011543472.1:c.465A>T	XP_011541774.1:p.Ile155=
XM_011543473.1:c.465A>T	XP_011541775.1:p.Ile155=
XM_011543474.1:c.435A>T	XP_011541776.1:p.Ile145=
XM_011543475.1:c.282A>T	XP_011541777.1:p.Ile94=
XM_011543476.1:c.228A>T	XP_011541778.1:p.Ile76=
XM_011543477.1:c.207A>T	XP_011541779.1:p.Ile69=
XM_011543478.1:c.144A>T	XP_011541780.1:p.Ile48=
XM_011543479.1:c.144A>T	XP_011541781.1:p.Ile48=
NM_001349241.1:c.435A>T	NP_001336170.1:p.Ile145=
NM_001349242.1:c.318A>T	NP_001336171.1:p.Ile106=
NM_001349243.1:c.-47A>T	NP_001336172.1:n.-47A>T
NM_001364599.1:c.465A>T	NP_001351528.1:p.Ile155=
NM_001364600.1:c.465A>T	NP_001351529.1:p.Ile155=
NM_001364602.1:c.456A>T	NP_001351531.1:p.Ile152=
NM_001364603.1:c.-303A>T	NP_001351532.1:n.-303A>T
NM_001364604.1:c.-47A>T	NP_001351533.1:n.-47A>T
XM_011543470.2:c.612A>T	XP_011541772.1:p.Ile204=
XM_011543471.2:c.465A>T	XP_011541773.1:p.Ile155=
XM_017009565.1:c.612A>T	XP_016865054.1:p.Ile204=
XM_017009566.1:c.465A>T	XP_016865055.1:p.Ile155=
XM_017009567.1:c.450A>T	XP_016865056.1:p.Ile150=
XM_024446110.1:c.612A>T	XP_024301878.1:p.Ile204=
XM_024446112.1:c.465A>T	XP_024301880.1:p.Ile155=
NM_001104631.2:c.648A>T MANE Select	NP_001098101.1:p.Ile216=
NM_001165899.2:c.465A>T	NP_001159371.1:p.Ile155=
NM_001197218.2:c.456A>T	NP_001184147.1:p.Ile152=
NM_001197219.2:c.282A>T	NP_001184148.1:p.Ile94=
NM_001197220.2:c.258A>T	NP_001184149.1:p.Ile86=
NM_001349241.2:c.435A>T	NP_001336170.1:p.Ile145=
NM_001349243.2:c.-47A>T	NP_001336172.1:n.-47A>T
NM_001364600.2:c.465A>T	NP_001351529.1:p.Ile155=
NM_001364602.2:c.456A>T	NP_001351531.1:p.Ile152=
NM_001349242.2:c.318A>T	NP_001336171.1:p.Ile106=
NM_006203.5:c.240A>T	NP_006194.2:p.Ile80=