Canonical Allele Identifier: CA812644082

Gene: PDE4D

Linked Data

• dbSNP Id: rs1382508472
• gnomAD v3: 5-59684077-C-A
• gnomAD v4: 5-59684077-C-A
• MyVariant Identifiers: chr5:g.58979903C>A (hg19) ; chr5:g.59684077C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.59684077C>A , CM000667.2:g.59684077C>A	GRCh38
NC_000005.9:g.58979903C>A , CM000667.1:g.58979903C>A	GRCh37
NC_000005.8:g.59015660C>A	NCBI36
NG_027957.1:g.809023G>T
NG_027957.2:g.845253G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000507116.6:c.263+84170G>T	ENSP00000424852.1:n.263+84170G>T
ENST00000340635.11:c.455+209091G>T MANE Select	ENSP00000345502.6:n.455+209091G>T
ENST00000309641.10:c.263+84170G>T	ENSP00000308485.6:n.263+84170G>T
ENST00000340635.10:c.455+209091G>T	ENSP00000345502.6:n.455+209091G>T
ENST00000405053.7:n.118+209091G>T
ENST00000502484.6:c.272+304411G>T	ENSP00000423094.2:n.272+304411G>T
ENST00000502575.1:c.263+84170G>T	ENSP00000425917.1:n.263+84170G>T
ENST00000507116.5:c.263+84170G>T	ENSP00000424852.1:n.263+84170G>T
ENST00000512069.6:n.218-123163G>T
ENST00000514231.1:n.218+112983G>T
NM_001104631.1:c.455+209091G>T	NP_001098101.1:n.455+209091G>T
NM_001165899.1:c.272+304411G>T	NP_001159371.1:n.272+304411G>T
NM_001197218.1:c.263+84170G>T	NP_001184147.1:n.263+84170G>T
XM_011543469.1:c.419+304411G>T	XP_011541771.1:n.419+304411G>T
XM_011543470.1:c.419+304411G>T	XP_011541772.1:n.419+304411G>T
XM_011543471.1:c.272+304411G>T	XP_011541773.1:n.272+304411G>T
XM_011543472.1:c.272+304411G>T	XP_011541774.1:n.272+304411G>T
XM_011543473.1:c.272+304411G>T	XP_011541775.1:n.272+304411G>T
XM_011543474.1:c.242+304411G>T	XP_011541776.1:n.242+304411G>T
XM_011543477.1:c.14+112983G>T	XP_011541779.1:n.14+112983G>T
NM_001349241.1:c.242+304411G>T	NP_001336170.1:n.242+304411G>T
NM_001349243.1:c.-240+304411G>T	NP_001336172.1:n.-240+304411G>T
NM_001364599.1:c.272+304411G>T	NP_001351528.1:n.272+304411G>T
NM_001364600.1:c.272+304411G>T	NP_001351529.1:n.272+304411G>T
NM_001364601.1:c.263+84170G>T	NP_001351530.1:n.263+84170G>T
NM_001364602.1:c.263+84170G>T	NP_001351531.1:n.263+84170G>T
NM_001364603.1:c.-496+84170G>T	NP_001351532.1:n.-496+84170G>T
XM_011543470.2:c.419+304411G>T	XP_011541772.1:n.419+304411G>T
XM_011543471.2:c.272+304411G>T	XP_011541773.1:n.272+304411G>T
XM_017009565.1:c.419+304411G>T	XP_016865054.1:n.419+304411G>T
XM_017009566.1:c.272+304411G>T	XP_016865055.1:n.272+304411G>T
XM_017009567.1:c.257+304411G>T	XP_016865056.1:n.257+304411G>T
XM_024446110.1:c.419+304411G>T	XP_024301878.1:n.419+304411G>T
XM_024446112.1:c.272+304411G>T	XP_024301880.1:n.272+304411G>T
NM_001104631.2:c.455+209091G>T MANE Select	NP_001098101.1:n.455+209091G>T
NM_001165899.2:c.272+304411G>T	NP_001159371.1:n.272+304411G>T
NM_001197218.2:c.263+84170G>T	NP_001184147.1:n.263+84170G>T
NM_001349241.2:c.242+304411G>T	NP_001336170.1:n.242+304411G>T
NM_001349243.2:c.-240+304411G>T	NP_001336172.1:n.-240+304411G>T
NM_001364600.2:c.272+304411G>T	NP_001351529.1:n.272+304411G>T
NM_001364602.2:c.263+84170G>T	NP_001351531.1:n.263+84170G>T