Canonical Allele Identifier: CA1953917096

Gene: PDE3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14752901_14752908delinsCTTTTGCT , CM000673.2:g.14752901_14752908delinsCTTTTGCT	GRCh38
NC_000011.9:g.14774447_14774454delinsCTTTTGCT , CM000673.1:g.14774447_14774454delinsCTTTTGCT	GRCh37
NC_000011.8:g.14731023_14731030delinsCTTTTGCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282096.9:c.979-19036_979-19029delinsCTTTTGCT MANE Select	ENSP00000282096.4:n.979-19036_979-19029delinsCTTTTGCT
ENST00000282096.8:c.979-19036_979-19029delinsCTTTTGCT	ENSP00000282096.4:n.979-19036_979-19029delinsCTTTTGCT
ENST00000455098.2:c.979-19036_979-19029delinsCTTTTGCT	ENSP00000388644.2:n.979-19036_979-19029delinsCTTTTGCT
ENST00000534317.1:n.795-19036_795-19029delinsCTTTTGCT
NM_000922.3:c.979-19036_979-19029delinsCTTTTGCT	NP_000913.2:n.979-19036_979-19029delinsCTTTTGCT
XM_006718249.2:c.979-19036_979-19029delinsCTTTTGCT	XP_006718312.1:n.979-19036_979-19029delinsCTTTTGCT
XM_011520183.1:c.979-19036_979-19029delinsCTTTTGCT	XP_011518485.1:n.979-19036_979-19029delinsCTTTTGCT
NM_001363569.1:c.979-19036_979-19029delinsCTTTTGCT	NP_001350498.1:n.979-19036_979-19029delinsCTTTTGCT
NM_001363570.1:c.979-19036_979-19029delinsCTTTTGCT	NP_001350499.1:n.979-19036_979-19029delinsCTTTTGCT
XM_006718249.3:c.979-19036_979-19029delinsCTTTTGCT	XP_006718312.1:n.979-19036_979-19029delinsCTTTTGCT
XM_017017911.2:c.979-19036_979-19029delinsCTTTTGCT	XP_016873400.1:n.979-19036_979-19029delinsCTTTTGCT
XM_017017912.1:c.979-19036_979-19029delinsCTTTTGCT	XP_016873401.1:n.979-19036_979-19029delinsCTTTTGCT
XR_001747903.2:n.1364-19036_1364-19029delinsCTTTTGCT
NM_000922.4:c.979-19036_979-19029delinsCTTTTGCT MANE Select	NP_000913.2:n.979-19036_979-19029delinsCTTTTGCT
NM_001363569.2:c.979-19036_979-19029delinsCTTTTGCT	NP_001350498.1:n.979-19036_979-19029delinsCTTTTGCT
NM_001363570.2:c.979-19036_979-19029delinsCTTTTGCT	NP_001350499.1:n.979-19036_979-19029delinsCTTTTGCT