Canonical Allele Identifier: CA9194826
Gene: PDE4A HGNC NCBI

Linked Data

dbSNP Id: rs4804134

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10457843T>G , CM000681.2:g.10457843T>G GRCh38
NC_000019.9:g.10568519T>G , CM000681.1:g.10568519T>G GRCh37
NC_000019.8:g.10429519T>G NCBI36
NG_029594.1:g.46071T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000380702.7:c.878-36T>G MANE Select ENSP00000370078.3:n.878-36T>G
ENST00000293683.9:n.800-36T>G ENSP00000293683.4:n.800-36T>G
ENST00000344979.7:c.161-36T>G ENSP00000341007.2:n.161-36T>G
ENST00000380702.6:c.878-36T>G ENSP00000370078.3:n.878-36T>G
ENST00000440014.6:n.695-36T>G ENSP00000394754.1:n.695-36T>G
ENST00000586275.1:n.141-36T>G
ENST00000589073.1:c.160+2921T>G ENSP00000465792.1:n.160+2921T>G
ENST00000591971.5:n.206-36T>G ENSP00000467137.1:n.206-36T>G
ENST00000592685.5:c.812-36T>G ENSP00000468507.1:n.812-36T>G
NM_001111307.1:c.878-36T>G NP_001104777.1:n.878-36T>G
NM_001111308.1:n.800-36T>G NP_001104778.1:n.800-36T>G
NM_001111309.1:n.695-36T>G NP_001104779.1:n.695-36T>G
NM_001243121.1:c.812-36T>G NP_001230050.1:n.812-36T>G
NM_006202.2:c.161-36T>G NP_006193.1:n.161-36T>G
XM_005259933.2:c.-35-36T>G XP_005259990.1:n.-35-36T>G
XM_011528054.1:c.812-36T>G XP_011526356.1:n.812-36T>G
XM_011528055.1:c.878-36T>G XP_011526357.1:n.878-36T>G
XM_011528055.3:c.878-36T>G XP_011526357.1:n.878-36T>G
XM_017026865.2:c.875-36T>G XP_016882354.1:n.875-36T>G
XM_024451534.1:c.-35-36T>G XP_024307302.1:n.-35-36T>G
NM_001111307.2:c.878-36T>G MANE Select NP_001104777.1:n.878-36T>G
NM_006202.3:c.161-36T>G NP_006193.1:n.161-36T>G
NM_001243121.2:c.812-36T>G NP_001230050.1:n.812-36T>G