Canonical Allele Identifier: CA673975383

Gene: PDE3B

Linked Data

• dbSNP Id: rs1454656662
• MyVariant Identifiers: chr11:g.14774439_14774440insA (hg19) ; chr11:g.14752893_14752894insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14752893_14752894insA , CM000673.2:g.14752893_14752894insA	GRCh38
NC_000011.9:g.14774439_14774440insA , CM000673.1:g.14774439_14774440insA	GRCh37
NC_000011.8:g.14731015_14731016insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282096.9:c.979-19044_979-19043insA MANE Select	ENSP00000282096.4:n.979-19044_979-19043insA
ENST00000282096.8:c.979-19044_979-19043insA	ENSP00000282096.4:n.979-19044_979-19043insA
ENST00000455098.2:c.979-19044_979-19043insA	ENSP00000388644.2:n.979-19044_979-19043insA
ENST00000534317.1:n.795-19044_795-19043insA
NM_000922.3:c.979-19044_979-19043insA	NP_000913.2:n.979-19044_979-19043insA
XM_006718249.2:c.979-19044_979-19043insA	XP_006718312.1:n.979-19044_979-19043insA
XM_011520183.1:c.979-19044_979-19043insA	XP_011518485.1:n.979-19044_979-19043insA
NM_001363569.1:c.979-19044_979-19043insA	NP_001350498.1:n.979-19044_979-19043insA
NM_001363570.1:c.979-19044_979-19043insA	NP_001350499.1:n.979-19044_979-19043insA
XM_006718249.3:c.979-19044_979-19043insA	XP_006718312.1:n.979-19044_979-19043insA
XM_017017911.2:c.979-19044_979-19043insA	XP_016873400.1:n.979-19044_979-19043insA
XM_017017912.1:c.979-19044_979-19043insA	XP_016873401.1:n.979-19044_979-19043insA
XR_001747903.2:n.1364-19044_1364-19043insA
NM_000922.4:c.979-19044_979-19043insA MANE Select	NP_000913.2:n.979-19044_979-19043insA
NM_001363569.2:c.979-19044_979-19043insA	NP_001350498.1:n.979-19044_979-19043insA
NM_001363570.2:c.979-19044_979-19043insA	NP_001350499.1:n.979-19044_979-19043insA