Canonical Allele Identifier: CA1549769529
Gene: PDE4D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60414032_60414033delinsAC , CM000667.2:g.60414032_60414033delinsAC GRCh38
NC_000005.9:g.59709859_59709860delinsAC , CM000667.1:g.59709859_59709860delinsAC GRCh37
NC_000005.8:g.59745616_59745617delinsAC NCBI36
NG_027957.1:g.79066_79067delinsGT
NG_027957.2:g.115297_115298delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000502484.6:c.-90+73909_-90+73910delinsGT ENSP00000423094.2:n.-90+73909_-90+73910delinsGT
ENST00000505507.6:c.-213+73909_-213+73910delinsGT ENSP00000425910.2:n.-213+73909_-213+73910delinsGT
ENST00000506024.5:n.71+34604_71+34605delinsGT
ENST00000506510.6:n.70+108018_70+108019delinsGT
ENST00000509355.5:n.157+73909_157+73910delinsGT
ENST00000511382.1:n.124+73909_124+73910delinsGT
ENST00000515835.2:c.-213+73909_-213+73910delinsGT ENSP00000424281.2:n.-213+73909_-213+73910delinsGT
NM_001165899.1:c.-90+73909_-90+73910delinsGT NP_001159371.1:n.-90+73909_-90+73910delinsGT
XM_011543472.1:c.-90+108018_-90+108019delinsGT XP_011541774.1:n.-90+108018_-90+108019delinsGT
XM_011543473.1:c.-90+34604_-90+34605delinsGT XP_011541775.1:n.-90+34604_-90+34605delinsGT
NM_001349241.1:c.-193+73909_-193+73910delinsGT NP_001336170.1:n.-193+73909_-193+73910delinsGT
NM_001349243.1:c.-674+73909_-674+73910delinsGT NP_001336172.1:n.-674+73909_-674+73910delinsGT
NM_001364599.1:c.-90+82106_-90+82107delinsGT NP_001351528.1:n.-90+82106_-90+82107delinsGT
XM_017009566.1:c.-139+73909_-139+73910delinsGT XP_016865055.1:n.-139+73909_-139+73910delinsGT
XM_024446110.1:c.-90+108018_-90+108019delinsGT XP_024301878.1:n.-90+108018_-90+108019delinsGT
XM_024446112.1:c.-90+108018_-90+108019delinsGT XP_024301880.1:n.-90+108018_-90+108019delinsGT
NM_001165899.2:c.-90+73909_-90+73910delinsGT NP_001159371.1:n.-90+73909_-90+73910delinsGT
NM_001349241.2:c.-193+73909_-193+73910delinsGT NP_001336170.1:n.-193+73909_-193+73910delinsGT
NM_001349243.2:c.-674+73909_-674+73910delinsGT NP_001336172.1:n.-674+73909_-674+73910delinsGT