Canonical Allele Identifier: CA1172569408

Gene: PDE4B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.66092938C= , CM000663.2:g.66092938C=	GRCh38
NC_000001.10:g.66558621C= , CM000663.1:g.66558621C=	GRCh37
NC_000001.9:g.66331209C=	NCBI36
NG_029038.1:g.305429C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341517.9:c.282-154522C= MANE Select	ENSP00000342637.4:n.282-154522C=
ENST00000329654.8:c.282-154522C=	ENSP00000332116.4:n.282-154522C=
ENST00000341517.8:c.282-154522C=	ENSP00000342637.4:n.282-154522C=
ENST00000423207.6:c.236+99796C=	ENSP00000392947.2:n.236+99796C=
ENST00000526666.1:n.473+44048C=
ENST00000531358.1:n.528-19832C=
ENST00000532040.1:n.472+29981C=
NM_001037340.2:c.236+99796C=	NP_001032417.1:n.236+99796C=
NM_001037341.1:c.282-154522C=	NP_001032418.1:n.282-154522C=
NM_001297440.1:c.6-154522C=	NP_001284369.1:n.6-154522C=
NM_001297441.1:c.56+52230C=	NP_001284370.1:n.56+52230C=
NM_002600.3:c.282-154522C=	NP_002591.2:n.282-154522C=
XM_011541565.1:c.17+44048C=	XP_011539867.1:n.17+44048C=
XM_011541566.1:c.-287-154522C=	XP_011539868.1:n.-287-154522C=
NM_002600.4:c.282-154522C= MANE Select	NP_002591.2:n.282-154522C=
NM_001037340.3:c.236+99796C=	NP_001032417.1:n.236+99796C=
NM_001037341.2:c.282-154522C=	NP_001032418.1:n.282-154522C=
NM_001297440.2:c.6-154522C=	NP_001284369.1:n.6-154522C=