Canonical Allele Identifier: CA1549769428
Gene: PDE4D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60413786_60413787delinsTG , CM000667.2:g.60413786_60413787delinsTG GRCh38
NC_000005.9:g.59709613_59709614delinsTG , CM000667.1:g.59709613_59709614delinsTG GRCh37
NC_000005.8:g.59745370_59745371delinsTG NCBI36
NG_027957.1:g.79312_79313delinsCA
NG_027957.2:g.115543_115544delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000502484.6:c.-90+74155_-90+74156delinsCA ENSP00000423094.2:n.-90+74155_-90+74156delinsCA
ENST00000505507.6:c.-213+74155_-213+74156delinsCA ENSP00000425910.2:n.-213+74155_-213+74156delinsCA
ENST00000506024.5:n.71+34850_71+34851delinsCA
ENST00000506510.6:n.70+108264_70+108265delinsCA
ENST00000509355.5:n.157+74155_157+74156delinsCA
ENST00000511382.1:n.124+74155_124+74156delinsCA
ENST00000515835.2:c.-213+74155_-213+74156delinsCA ENSP00000424281.2:n.-213+74155_-213+74156delinsCA
NM_001165899.1:c.-90+74155_-90+74156delinsCA NP_001159371.1:n.-90+74155_-90+74156delinsCA
XM_011543472.1:c.-90+108264_-90+108265delinsCA XP_011541774.1:n.-90+108264_-90+108265delinsCA
XM_011543473.1:c.-90+34850_-90+34851delinsCA XP_011541775.1:n.-90+34850_-90+34851delinsCA
NM_001349241.1:c.-193+74155_-193+74156delinsCA NP_001336170.1:n.-193+74155_-193+74156delinsCA
NM_001349243.1:c.-674+74155_-674+74156delinsCA NP_001336172.1:n.-674+74155_-674+74156delinsCA
NM_001364599.1:c.-90+82352_-90+82353delinsCA NP_001351528.1:n.-90+82352_-90+82353delinsCA
XM_017009566.1:c.-139+74155_-139+74156delinsCA XP_016865055.1:n.-139+74155_-139+74156delinsCA
XM_024446110.1:c.-90+108264_-90+108265delinsCA XP_024301878.1:n.-90+108264_-90+108265delinsCA
XM_024446112.1:c.-90+108264_-90+108265delinsCA XP_024301880.1:n.-90+108264_-90+108265delinsCA
NM_001165899.2:c.-90+74155_-90+74156delinsCA NP_001159371.1:n.-90+74155_-90+74156delinsCA
NM_001349241.2:c.-193+74155_-193+74156delinsCA NP_001336170.1:n.-193+74155_-193+74156delinsCA
NM_001349243.2:c.-674+74155_-674+74156delinsCA NP_001336172.1:n.-674+74155_-674+74156delinsCA