Canonical Allele Identifier: CA16228637
Gene: PDE4D HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs181736

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.59381407G>A , CM000667.2:g.59381407G>A GRCh38
NC_000005.8:g.58712990G>A NCBI36
NC_000005.9:g.58677233G>A , CM000667.1:g.58677233G>A GRCh37
NG_027957.1:g.1111693C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000309641.10:n.264-165439C>T ENSP00000308485.6:p.=
ENST00000340635.10:c.456-165439C>T ENSP00000345502.6:p.=
ENST00000360047.9:c.48-165439C>T ENSP00000353152.5:p.=
ENST00000405053.7:n.119-165439C>T
ENST00000502484.6:c.273-165439C>T ENSP00000423094.2:p.=
ENST00000502575.1:c.264-165439C>T ENSP00000425917.1:p.=
ENST00000505453.1:c.-99+204922C>T ENSP00000421013.1:p.=
ENST00000507116.5:c.264-165439C>T ENSP00000424852.1:p.=
ENST00000514231.1:n.219-165439C>T
NM_001104631.1:c.456-165439C>T VV NP_001098101.1:p.=
NM_001165899.1:c.273-165439C>T VV NP_001159371.1:p.=
NM_001197218.1:c.264-165439C>T VV NP_001184147.1:p.=
NM_006203.4:c.48-165439C>T VV NP_006194.2:p.=
XM_005248537.2:c.125+48887C>T XP_005248594.1:p.=
XM_005248538.3:c.48-165439C>T XP_005248595.1:p.=
XM_011543469.1:c.420-165439C>T XP_011541771.1:p.=
XM_011543470.1:c.420-165439C>T XP_011541772.1:p.=
XM_011543471.1:c.273-165439C>T XP_011541773.1:p.=
XM_011543472.1:c.273-165439C>T XP_011541774.1:p.=
XM_011543473.1:c.273-165439C>T XP_011541775.1:p.=
XM_011543474.1:c.243-165439C>T XP_011541776.1:p.=
XM_011543475.1:c.89+148920C>T XP_011541777.1:p.=
XM_011543476.1:c.35+53035C>T XP_011541778.1:p.=
XM_011543477.1:c.15-165439C>T XP_011541779.1:p.=
XM_011543478.1:c.-50+1363C>T XP_011541780.1:p.=