Canonical Allele Identifier: CA1549802461
Gene: PDE4D HGNC NCBI

Linked Data

dbSNP Id: rs1749242737

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60487462C>T , CM000667.2:g.60487462C>T GRCh38
NC_000005.9:g.59783289C>T , CM000667.1:g.59783289C>T GRCh37
NC_000005.8:g.59819046C>T NCBI36
NG_027957.1:g.5637G>A
NG_027957.2:g.41868G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000502484.6:c.-90+480G>A ENSP00000423094.2:n.-90+480G>A
ENST00000505507.6:c.-213+480G>A ENSP00000425910.2:n.-213+480G>A
ENST00000506510.6:n.70+34589G>A
ENST00000509355.5:n.157+480G>A
ENST00000511382.1:n.124+480G>A
ENST00000515835.2:c.-213+480G>A ENSP00000424281.2:n.-213+480G>A
NM_001165899.1:c.-90+480G>A NP_001159371.1:n.-90+480G>A
XM_011543472.1:c.-90+34589G>A XP_011541774.1:n.-90+34589G>A
NM_001349241.1:c.-193+480G>A NP_001336170.1:n.-193+480G>A
NM_001349243.1:c.-674+480G>A NP_001336172.1:n.-674+480G>A
NM_001364599.1:c.-90+8677G>A NP_001351528.1:n.-90+8677G>A
XM_017009566.1:c.-139+480G>A XP_016865055.1:n.-139+480G>A
XM_024446110.1:c.-90+34589G>A XP_024301878.1:n.-90+34589G>A
XM_024446112.1:c.-90+34589G>A XP_024301880.1:n.-90+34589G>A
NM_001165899.2:c.-90+480G>A NP_001159371.1:n.-90+480G>A
NM_001349241.2:c.-193+480G>A NP_001336170.1:n.-193+480G>A
NM_001349243.2:c.-674+480G>A NP_001336172.1:n.-674+480G>A