Canonical Allele Identifier: CA1549802436
Gene: PDE4D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60487420_60487421delinsAT , CM000667.2:g.60487420_60487421delinsAT GRCh38
NC_000005.9:g.59783247_59783248delinsAT , CM000667.1:g.59783247_59783248delinsAT GRCh37
NC_000005.8:g.59819004_59819005delinsAT NCBI36
NG_027957.1:g.5678_5679delinsAT
NG_027957.2:g.41909_41910delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000502484.6:c.-90+521_-90+522delinsAT ENSP00000423094.2:n.-90+521_-90+522delinsAT
ENST00000505507.6:c.-213+521_-213+522delinsAT ENSP00000425910.2:n.-213+521_-213+522delinsAT
ENST00000506510.6:n.70+34630_70+34631delinsAT
ENST00000509355.5:n.157+521_157+522delinsAT
ENST00000511382.1:n.124+521_124+522delinsAT
ENST00000515835.2:c.-213+521_-213+522delinsAT ENSP00000424281.2:n.-213+521_-213+522delinsAT
NM_001165899.1:c.-90+521_-90+522delinsAT NP_001159371.1:n.-90+521_-90+522delinsAT
XM_011543472.1:c.-90+34630_-90+34631delinsAT XP_011541774.1:n.-90+34630_-90+34631delinsAT
NM_001349241.1:c.-193+521_-193+522delinsAT NP_001336170.1:n.-193+521_-193+522delinsAT
NM_001349243.1:c.-674+521_-674+522delinsAT NP_001336172.1:n.-674+521_-674+522delinsAT
NM_001364599.1:c.-90+8718_-90+8719delinsAT NP_001351528.1:n.-90+8718_-90+8719delinsAT
XM_017009566.1:c.-139+521_-139+522delinsAT XP_016865055.1:n.-139+521_-139+522delinsAT
XM_024446110.1:c.-90+34630_-90+34631delinsAT XP_024301878.1:n.-90+34630_-90+34631delinsAT
XM_024446112.1:c.-90+34630_-90+34631delinsAT XP_024301880.1:n.-90+34630_-90+34631delinsAT
NM_001165899.2:c.-90+521_-90+522delinsAT NP_001159371.1:n.-90+521_-90+522delinsAT
NM_001349241.2:c.-193+521_-193+522delinsAT NP_001336170.1:n.-193+521_-193+522delinsAT
NM_001349243.2:c.-674+521_-674+522delinsAT NP_001336172.1:n.-674+521_-674+522delinsAT