Canonical Allele Identifier: CA1549769477
Gene: PDE4D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60413900G= , CM000667.2:g.60413900G= GRCh38
NC_000005.9:g.59709727G= , CM000667.1:g.59709727G= GRCh37
NC_000005.8:g.59745484G= NCBI36
NG_027957.1:g.79199C=
NG_027957.2:g.115430C=

Transcript Alleles

HGVS Amino-acid change
ENST00000502484.6:c.-90+74042C= ENSP00000423094.2:n.-90+74042C=
ENST00000505507.6:c.-213+74042C= ENSP00000425910.2:n.-213+74042C=
ENST00000506024.5:n.71+34737C=
ENST00000506510.6:n.70+108151C=
ENST00000509355.5:n.157+74042C=
ENST00000511382.1:n.124+74042C=
ENST00000515835.2:c.-213+74042C= ENSP00000424281.2:n.-213+74042C=
NM_001165899.1:c.-90+74042C= NP_001159371.1:n.-90+74042C=
XM_011543472.1:c.-90+108151C= XP_011541774.1:n.-90+108151C=
XM_011543473.1:c.-90+34737C= XP_011541775.1:n.-90+34737C=
NM_001349241.1:c.-193+74042C= NP_001336170.1:n.-193+74042C=
NM_001349243.1:c.-674+74042C= NP_001336172.1:n.-674+74042C=
NM_001364599.1:c.-90+82239C= NP_001351528.1:n.-90+82239C=
XM_017009566.1:c.-139+74042C= XP_016865055.1:n.-139+74042C=
XM_024446110.1:c.-90+108151C= XP_024301878.1:n.-90+108151C=
XM_024446112.1:c.-90+108151C= XP_024301880.1:n.-90+108151C=
NM_001165899.2:c.-90+74042C= NP_001159371.1:n.-90+74042C=
NM_001349241.2:c.-193+74042C= NP_001336170.1:n.-193+74042C=
NM_001349243.2:c.-674+74042C= NP_001336172.1:n.-674+74042C=