Canonical Allele Identifier: CA2838318175

Gene: PDE4B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.66329786G>T , CM000663.2:g.66329786G>T	GRCh38
NC_000001.10:g.66795469G>T , CM000663.1:g.66795469G>T	GRCh37
NC_000001.9:g.66568057G>T	NCBI36
NG_029038.1:g.542277G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341517.9:c.635-2722G>T MANE Select	ENSP00000342637.4:n.635-2722G>T
ENST00000329654.8:c.635-2722G>T	ENSP00000332116.4:n.635-2722G>T
ENST00000341517.8:c.635-2722G>T	ENSP00000342637.4:n.635-2722G>T
ENST00000412480.6:c.359-2722G>T	ENSP00000397548.2:n.359-2722G>T
ENST00000423207.6:c.590-2722G>T	ENSP00000392947.2:n.590-2722G>T
NM_001037340.2:c.590-2722G>T	NP_001032417.1:n.590-2722G>T
NM_001037341.1:c.635-2722G>T	NP_001032418.1:n.635-2722G>T
NM_001297440.1:c.359-2722G>T	NP_001284369.1:n.359-2722G>T
NM_001297441.1:c.410-2722G>T	NP_001284370.1:n.410-2722G>T
NM_002600.3:c.635-2722G>T	NP_002591.2:n.635-2722G>T
XM_011541565.1:c.371-2722G>T	XP_011539867.1:n.371-2722G>T
XM_011541566.1:c.17-2722G>T	XP_011539868.1:n.17-2722G>T
XM_017001445.1:c.218-2722G>T	XP_016856934.1:n.218-2722G>T
NM_002600.4:c.635-2722G>T MANE Select	NP_002591.2:n.635-2722G>T
NM_001037340.3:c.590-2722G>T	NP_001032417.1:n.590-2722G>T
NM_001037341.2:c.635-2722G>T	NP_001032418.1:n.635-2722G>T
NM_001297440.2:c.359-2722G>T	NP_001284369.1:n.359-2722G>T