Canonical Allele Identifier: CA523730601

Gene: PDE4B

Linked Data

• dbSNP Id: rs1349671059
• gnomAD v2: 1-66558728-AG-A
• MyVariant Identifiers: chr1:g.66558729del (hg19) ; chr1:g.66093046del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.66093048del , CM000663.2:g.66093048del	GRCh38
NC_000001.10:g.66558731del , CM000663.1:g.66558731del	GRCh37
NC_000001.9:g.66331319del	NCBI36
NG_029038.1:g.305539del

Transcript Alleles

HGVS	Amino-acid change
ENST00000341517.9:c.282-154412del MANE Select	ENSP00000342637.4:n.282-154412del
ENST00000329654.8:c.282-154412del	ENSP00000332116.4:n.282-154412del
ENST00000341517.8:c.282-154412del	ENSP00000342637.4:n.282-154412del
ENST00000423207.6:c.236+99906del	ENSP00000392947.2:n.236+99906del
ENST00000526666.1:n.473+44158del
ENST00000531358.1:n.528-19722del
ENST00000532040.1:n.472+30091del
NM_001037340.2:c.236+99906del	NP_001032417.1:n.236+99906del
NM_001037341.1:c.282-154412del	NP_001032418.1:n.282-154412del
NM_001297440.1:c.6-154412del	NP_001284369.1:n.6-154412del
NM_001297441.1:c.56+52340del	NP_001284370.1:n.56+52340del
NM_002600.3:c.282-154412del	NP_002591.2:n.282-154412del
XM_011541565.1:c.17+44158del	XP_011539867.1:n.17+44158del
XM_011541566.1:c.-287-154412del	XP_011539868.1:n.-287-154412del
NM_002600.4:c.282-154412del MANE Select	NP_002591.2:n.282-154412del
NM_001037340.3:c.236+99906del	NP_001032417.1:n.236+99906del
NM_001037341.2:c.282-154412del	NP_001032418.1:n.282-154412del
NM_001297440.2:c.6-154412del	NP_001284369.1:n.6-154412del