Canonical Allele Identifier: CA15067955

Gene: PDE4B

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.66335081A>G , CM000663.2:g.66335081A>G	GRCh38
NC_000001.10:g.66800764A>G , CM000663.1:g.66800764A>G	GRCh37
NC_000001.9:g.66573352A>G	NCBI36
NG_029038.1:g.547572A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341517.9:c.747+2461A>G MANE Select	ENSP00000342637.4:n.747+2461A>G
ENST00000329654.8:c.747+2461A>G	ENSP00000332116.4:n.747+2461A>G
ENST00000341517.8:c.747+2461A>G	ENSP00000342637.4:n.747+2461A>G
ENST00000371045.9:c.231+2461A>G	ENSP00000360084.5:n.231+2461A>G
ENST00000423207.6:c.702+2461A>G	ENSP00000392947.2:n.702+2461A>G
ENST00000526197.5:c.90+2461A>G	ENSP00000436104.1:n.90+2461A>G
ENST00000528771.5:c.90+2461A>G	ENSP00000431909.1:n.90+2461A>G
ENST00000531025.5:c.90+2461A>G	ENSP00000437249.1:n.90+2461A>G
NM_001037339.2:c.231+2461A>G	NP_001032416.1:n.231+2461A>G
NM_001037340.2:c.702+2461A>G	NP_001032417.1:n.702+2461A>G
NM_001037341.1:c.747+2461A>G	NP_001032418.1:n.747+2461A>G
NM_001297440.1:c.471+2461A>G	NP_001284369.1:n.471+2461A>G
NM_001297441.1:c.522+2461A>G	NP_001284370.1:n.522+2461A>G
NM_002600.3:c.747+2461A>G	NP_002591.2:n.747+2461A>G
XM_005270923.3:c.156+2461A>G	XP_005270980.1:n.156+2461A>G
XM_005270924.3:c.90+2461A>G	XP_005270981.1:n.90+2461A>G
XM_005270925.2:c.90+2461A>G	XP_005270982.1:n.90+2461A>G
XM_006710680.2:c.132+2461A>G	XP_006710743.1:n.132+2461A>G
XM_011541565.1:c.483+2461A>G	XP_011539867.1:n.483+2461A>G
XM_011541566.1:c.129+2461A>G	XP_011539868.1:n.129+2461A>G
XM_006710680.3:c.132+2461A>G	XP_006710743.1:n.132+2461A>G
XM_017001445.1:c.330+2461A>G	XP_016856934.1:n.330+2461A>G
NM_002600.4:c.747+2461A>G MANE Select	NP_002591.2:n.747+2461A>G
NM_001037340.3:c.702+2461A>G	NP_001032417.1:n.702+2461A>G
NM_001037341.2:c.747+2461A>G	NP_001032418.1:n.747+2461A>G
NM_001297440.2:c.471+2461A>G	NP_001284369.1:n.471+2461A>G