Canonical Allele Identifier: CA935353513

Gene: PDE3B

Linked Data

• gnomAD v3: 11-14753081-TCCCC-T
• gnomAD v4: 11-14753081-TCCCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14753082_14753085del , CM000673.2:g.14753082_14753085del	GRCh38
NC_000011.9:g.14774628_14774631del , CM000673.1:g.14774628_14774631del	GRCh37
NC_000011.8:g.14731204_14731207del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282096.9:c.979-18855_979-18852del MANE Select	ENSP00000282096.4:n.979-18855_979-18852del
ENST00000282096.8:c.979-18855_979-18852del	ENSP00000282096.4:n.979-18855_979-18852del
ENST00000455098.2:c.979-18855_979-18852del	ENSP00000388644.2:n.979-18855_979-18852del
ENST00000534317.1:n.795-18855_795-18852del
NM_000922.3:c.979-18855_979-18852del	NP_000913.2:n.979-18855_979-18852del
XM_006718249.2:c.979-18855_979-18852del	XP_006718312.1:n.979-18855_979-18852del
XM_011520183.1:c.979-18855_979-18852del	XP_011518485.1:n.979-18855_979-18852del
NM_001363569.1:c.979-18855_979-18852del	NP_001350498.1:n.979-18855_979-18852del
NM_001363570.1:c.979-18855_979-18852del	NP_001350499.1:n.979-18855_979-18852del
XM_006718249.3:c.979-18855_979-18852del	XP_006718312.1:n.979-18855_979-18852del
XM_017017911.2:c.979-18855_979-18852del	XP_016873400.1:n.979-18855_979-18852del
XM_017017912.1:c.979-18855_979-18852del	XP_016873401.1:n.979-18855_979-18852del
XR_001747903.2:n.1364-18855_1364-18852del
NM_000922.4:c.979-18855_979-18852del MANE Select	NP_000913.2:n.979-18855_979-18852del
NM_001363569.2:c.979-18855_979-18852del	NP_001350498.1:n.979-18855_979-18852del
NM_001363570.2:c.979-18855_979-18852del	NP_001350499.1:n.979-18855_979-18852del