Canonical Allele Identifier: CA1140384802

Gene: PDE4B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.66281101G= , CM000663.2:g.66281101G=	GRCh38
NC_000001.10:g.66746784G= , CM000663.1:g.66746784G=	GRCh37
NC_000001.9:g.66519372G=	NCBI36
NG_029038.1:g.493592G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341517.9:c.634+15014G= MANE Select	ENSP00000342637.4:n.634+15014G=
ENST00000329654.8:c.634+15014G=	ENSP00000332116.4:n.634+15014G=
ENST00000341517.8:c.634+15014G=	ENSP00000342637.4:n.634+15014G=
ENST00000412480.6:c.358+15014G=	ENSP00000397548.2:n.358+15014G=
ENST00000423207.6:c.589+15014G=	ENSP00000392947.2:n.589+15014G=
NM_001037340.2:c.589+15014G=	NP_001032417.1:n.589+15014G=
NM_001037341.1:c.634+15014G=	NP_001032418.1:n.634+15014G=
NM_001297440.1:c.358+15014G=	NP_001284369.1:n.358+15014G=
NM_001297441.1:c.409+15014G=	NP_001284370.1:n.409+15014G=
NM_002600.3:c.634+15014G=	NP_002591.2:n.634+15014G=
XM_011541565.1:c.370+15014G=	XP_011539867.1:n.370+15014G=
XM_011541566.1:c.16+23238G=	XP_011539868.1:n.16+23238G=
XM_017001445.1:c.217+15014G=	XP_016856934.1:n.217+15014G=
NM_002600.4:c.634+15014G= MANE Select	NP_002591.2:n.634+15014G=
NM_001037340.3:c.589+15014G=	NP_001032417.1:n.589+15014G=
NM_001037341.2:c.634+15014G=	NP_001032418.1:n.634+15014G=
NM_001297440.2:c.358+15014G=	NP_001284369.1:n.358+15014G=