Canonical Allele Identifier: CA1172462455
Gene: PDE4B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.65845241_65845255delinsATTGTAAATAATTTG , CM000663.2:g.65845241_65845255delinsATTGTAAATAATTTG GRCh38
NC_000001.10:g.66310924_66310938delinsATTGTAAATAATTTG , CM000663.1:g.66310924_66310938delinsATTGTAAATAATTTG GRCh37
NC_000001.9:g.66083512_66083526delinsATTGTAAATAATTTG NCBI36
NG_029038.1:g.57732_57746delinsATTGTAAATAATTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000341517.9:c.-71+51993_-71+52007delinsATTGTAAATAATTTG MANE Select ENSP00000342637.4:n.-71+51993_-71+52007delinsATTGTAAATAATTTG
ENST00000329654.8:c.-71+52611_-71+52625delinsATTGTAAATAATTTG ENSP00000332116.4:n.-71+52611_-71+52625delinsATTGTAAATAATTTG
ENST00000341517.8:c.-71+51993_-71+52007delinsATTGTAAATAATTTG ENSP00000342637.4:n.-71+51993_-71+52007delinsATTGTAAATAATTTG
NM_001037341.1:c.-71+52611_-71+52625delinsATTGTAAATAATTTG NP_001032418.1:n.-71+52611_-71+52625delinsATTGTAAATAATTTG
NM_001297440.1:c.-108+52611_-108+52625delinsATTGTAAATAATTTG NP_001284369.1:n.-108+52611_-108+52625delinsATTGTAAATAATTTG
NM_002600.3:c.-71+51993_-71+52007delinsATTGTAAATAATTTG NP_002591.2:n.-71+51993_-71+52007delinsATTGTAAATAATTTG
NM_002600.4:c.-71+51993_-71+52007delinsATTGTAAATAATTTG MANE Select NP_002591.2:n.-71+51993_-71+52007delinsATTGTAAATAATTTG
NM_001037341.2:c.-71+52611_-71+52625delinsATTGTAAATAATTTG NP_001032418.1:n.-71+52611_-71+52625delinsATTGTAAATAATTTG
NM_001297440.2:c.-108+52611_-108+52625delinsATTGTAAATAATTTG NP_001284369.1:n.-108+52611_-108+52625delinsATTGTAAATAATTTG