Canonical Allele Identifier: CA1172462333
Gene: PDE4B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.65845088_65845090delinsCTA , CM000663.2:g.65845088_65845090delinsCTA GRCh38
NC_000001.10:g.66310771_66310773delinsCTA , CM000663.1:g.66310771_66310773delinsCTA GRCh37
NC_000001.9:g.66083359_66083361delinsCTA NCBI36
NG_029038.1:g.57579_57581delinsCTA

Transcript Alleles

HGVS Amino-acid change
ENST00000341517.9:c.-71+51840_-71+51842delinsCTA MANE Select ENSP00000342637.4:n.-71+51840_-71+51842de...
ENST00000329654.8:c.-71+52458_-71+52460delinsCTA ENSP00000332116.4:n.-71+52458_-71+52460de...
ENST00000341517.8:c.-71+51840_-71+51842delinsCTA ENSP00000342637.4:n.-71+51840_-71+51842de...
NM_001037341.1:c.-71+52458_-71+52460delinsCTA NP_001032418.1:n.-71+52458_-71+52460delin...
NM_001297440.1:c.-108+52458_-108+52460delinsCTA NP_001284369.1:n.-108+52458_-108+52460del...
NM_002600.3:c.-71+51840_-71+51842delinsCTA NP_002591.2:n.-71+51840_-71+51842delinsCT...
NM_002600.4:c.-71+51840_-71+51842delinsCTA MANE Select NP_002591.2:n.-71+51840_-71+51842delinsCT...
NM_001037341.2:c.-71+52458_-71+52460delinsCTA NP_001032418.1:n.-71+52458_-71+52460delin...
NM_001297440.2:c.-108+52458_-108+52460delinsCTA NP_001284369.1:n.-108+52458_-108+52460del...