Canonical Allele Identifier: CA1549769418
Gene: PDE4D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60413771T= , CM000667.2:g.60413771T= GRCh38
NC_000005.9:g.59709598T= , CM000667.1:g.59709598T= GRCh37
NC_000005.8:g.59745355T= NCBI36
NG_027957.1:g.79328A=
NG_027957.2:g.115559A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000502484.6:c.-90+74171A= ENSP00000423094.2:n.-90+74171A=
ENST00000505507.6:c.-213+74171A= ENSP00000425910.2:n.-213+74171A=
ENST00000506024.5:n.71+34866A=
ENST00000506510.6:n.70+108280A=
ENST00000509355.5:n.157+74171A=
ENST00000511382.1:n.124+74171A=
ENST00000515835.2:c.-213+74171A= ENSP00000424281.2:n.-213+74171A=
NM_001165899.1:c.-90+74171A= NP_001159371.1:n.-90+74171A=
XM_011543472.1:c.-90+108280A= XP_011541774.1:n.-90+108280A=
XM_011543473.1:c.-90+34866A= XP_011541775.1:n.-90+34866A=
NM_001349241.1:c.-193+74171A= NP_001336170.1:n.-193+74171A=
NM_001349243.1:c.-674+74171A= NP_001336172.1:n.-674+74171A=
NM_001364599.1:c.-90+82368A= NP_001351528.1:n.-90+82368A=
XM_017009566.1:c.-139+74171A= XP_016865055.1:n.-139+74171A=
XM_024446110.1:c.-90+108280A= XP_024301878.1:n.-90+108280A=
XM_024446112.1:c.-90+108280A= XP_024301880.1:n.-90+108280A=
NM_001165899.2:c.-90+74171A= NP_001159371.1:n.-90+74171A=
NM_001349241.2:c.-193+74171A= NP_001336170.1:n.-193+74171A=
NM_001349243.2:c.-674+74171A= NP_001336172.1:n.-674+74171A=