Canonical Allele Identifier: CA1172661687

Gene: PDE4B

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.66311907A>G , CM000663.2:g.66311907A>G	GRCh38
NC_000001.10:g.66777590A>G , CM000663.1:g.66777590A>G	GRCh37
NC_000001.9:g.66550178A>G	NCBI36
NG_029038.1:g.524398A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341517.9:c.635-20601A>G MANE Select	ENSP00000342637.4:n.635-20601A>G
ENST00000329654.8:c.635-20601A>G	ENSP00000332116.4:n.635-20601A>G
ENST00000341517.8:c.635-20601A>G	ENSP00000342637.4:n.635-20601A>G
ENST00000412480.6:c.359-20601A>G	ENSP00000397548.2:n.359-20601A>G
ENST00000423207.6:c.590-20601A>G	ENSP00000392947.2:n.590-20601A>G
NM_001037340.2:c.590-20601A>G	NP_001032417.1:n.590-20601A>G
NM_001037341.1:c.635-20601A>G	NP_001032418.1:n.635-20601A>G
NM_001297440.1:c.359-20601A>G	NP_001284369.1:n.359-20601A>G
NM_001297441.1:c.410-20601A>G	NP_001284370.1:n.410-20601A>G
NM_002600.3:c.635-20601A>G	NP_002591.2:n.635-20601A>G
XM_011541565.1:c.371-20601A>G	XP_011539867.1:n.371-20601A>G
XM_011541566.1:c.17-20601A>G	XP_011539868.1:n.17-20601A>G
XM_017001445.1:c.218-20601A>G	XP_016856934.1:n.218-20601A>G
NM_002600.4:c.635-20601A>G MANE Select	NP_002591.2:n.635-20601A>G
NM_001037340.3:c.590-20601A>G	NP_001032417.1:n.590-20601A>G
NM_001037341.2:c.635-20601A>G	NP_001032418.1:n.635-20601A>G
NM_001297440.2:c.359-20601A>G	NP_001284369.1:n.359-20601A>G