Canonical Allele Identifier: CA359930625

Gene: PDE4D

Linked Data

• MyVariant Identifiers: chr5:g.58511609C>A (hg19) ; chr5:g.59215783C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.59215783C>A , CM000667.2:g.59215783C>A	GRCh38
NC_000005.9:g.58511609C>A , CM000667.1:g.58511609C>A	GRCh37
NC_000005.8:g.58547366C>A	NCBI36
NG_027957.1:g.1277317G>T
NG_027957.2:g.1313547G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507116.6:c.449G>T	ENSP00000424852.1:p.Ser150Ile
ENST00000340635.11:c.641G>T MANE Select	ENSP00000345502.6:p.Ser214Ile
ENST00000636120.1:c.311G>T	ENSP00000490821.1:p.Ser104Ile
ENST00000638939.1:c.206G>T	ENSP00000492052.1:p.Ser69Ile
ENST00000309641.10:c.449G>T	ENSP00000308485.6:p.Ser150Ile
ENST00000340635.10:c.641G>T	ENSP00000345502.6:p.Ser214Ile
ENST00000360047.9:c.233G>T	ENSP00000353152.5:p.Ser78Ile
ENST00000405053.7:n.304G>T
ENST00000405755.6:c.275G>T	ENSP00000384806.2:p.Ser92Ile
ENST00000502484.6:c.458G>T	ENSP00000423094.2:p.Ser153Ile
ENST00000502575.1:c.449G>T	ENSP00000425917.1:p.Ser150Ile
ENST00000503258.5:c.251G>T	ENSP00000425605.1:p.Ser84Ile
ENST00000505453.1:c.-98-176812G>T	ENSP00000421013.1:n.-98-176812G>T
ENST00000507116.5:c.449G>T	ENSP00000424852.1:p.Ser150Ile
ENST00000514231.1:n.404G>T
ENST00000515324.1:n.153G>T
ENST00000546160.5:c.248G>T	ENSP00000442734.2:p.Ser83Ile
ENST00000621323.4:n.186G>T
NM_001104631.1:c.641G>T	NP_001098101.1:p.Ser214Ile
NM_001165899.1:c.458G>T	NP_001159371.1:p.Ser153Ile
NM_001197218.1:c.449G>T	NP_001184147.1:p.Ser150Ile
NM_001197219.1:c.275G>T	NP_001184148.1:p.Ser92Ile
NM_001197220.1:c.251G>T	NP_001184149.1:p.Ser84Ile
NM_006203.4:c.233G>T	NP_006194.2:p.Ser78Ile
XM_005248537.2:c.311G>T	XP_005248594.1:p.Ser104Ile
XM_005248538.3:c.233G>T	XP_005248595.1:p.Ser78Ile
XM_011543469.1:c.605G>T	XP_011541771.1:p.Ser202Ile
XM_011543470.1:c.605G>T	XP_011541772.1:p.Ser202Ile
XM_011543471.1:c.458G>T	XP_011541773.1:p.Ser153Ile
XM_011543472.1:c.458G>T	XP_011541774.1:p.Ser153Ile
XM_011543473.1:c.458G>T	XP_011541775.1:p.Ser153Ile
XM_011543474.1:c.428G>T	XP_011541776.1:p.Ser143Ile
XM_011543475.1:c.275G>T	XP_011541777.1:p.Ser92Ile
XM_011543476.1:c.221G>T	XP_011541778.1:p.Ser74Ile
XM_011543477.1:c.200G>T	XP_011541779.1:p.Ser67Ile
XM_011543478.1:c.137G>T	XP_011541780.1:p.Ser46Ile
XM_011543479.1:c.137G>T	XP_011541781.1:p.Ser46Ile
NM_001349241.1:c.428G>T	NP_001336170.1:p.Ser143Ile
NM_001349242.1:c.311G>T	NP_001336171.1:p.Ser104Ile
NM_001349243.1:c.-54G>T	NP_001336172.1:n.-54G>T
NM_001364599.1:c.458G>T	NP_001351528.1:p.Ser153Ile
NM_001364600.1:c.458G>T	NP_001351529.1:p.Ser153Ile
NM_001364601.1:c.449G>T	NP_001351530.1:p.Ser150Ile
NM_001364602.1:c.449G>T	NP_001351531.1:p.Ser150Ile
NM_001364603.1:c.-310G>T	NP_001351532.1:n.-310G>T
NM_001364604.1:c.-54G>T	NP_001351533.1:n.-54G>T
XM_011543470.2:c.605G>T	XP_011541772.1:p.Ser202Ile
XM_011543471.2:c.458G>T	XP_011541773.1:p.Ser153Ile
XM_017009565.1:c.605G>T	XP_016865054.1:p.Ser202Ile
XM_017009566.1:c.458G>T	XP_016865055.1:p.Ser153Ile
XM_017009567.1:c.443G>T	XP_016865056.1:p.Ser148Ile
XM_024446110.1:c.605G>T	XP_024301878.1:p.Ser202Ile
XM_024446112.1:c.458G>T	XP_024301880.1:p.Ser153Ile
NM_001104631.2:c.641G>T MANE Select	NP_001098101.1:p.Ser214Ile
NM_001165899.2:c.458G>T	NP_001159371.1:p.Ser153Ile
NM_001197218.2:c.449G>T	NP_001184147.1:p.Ser150Ile
NM_001197219.2:c.275G>T	NP_001184148.1:p.Ser92Ile
NM_001197220.2:c.251G>T	NP_001184149.1:p.Ser84Ile
NM_001349241.2:c.428G>T	NP_001336170.1:p.Ser143Ile
NM_001349243.2:c.-54G>T	NP_001336172.1:n.-54G>T
NM_001364600.2:c.458G>T	NP_001351529.1:p.Ser153Ile
NM_001364602.2:c.449G>T	NP_001351531.1:p.Ser150Ile
NM_001349242.2:c.311G>T	NP_001336171.1:p.Ser104Ile
NM_006203.5:c.233G>T	NP_006194.2:p.Ser78Ile