Canonical Allele Identifier: CA2559218835

Gene: PDE4B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.65845212_65845213del , CM000663.2:g.65845212_65845213del	GRCh38
NC_000001.10:g.66310895_66310896del , CM000663.1:g.66310895_66310896del	GRCh37
NC_000001.9:g.66083483_66083484del	NCBI36
NG_029038.1:g.57703_57704del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341517.9:c.-71+51964_-71+51965del MANE Select	ENSP00000342637.4:n.-71+51964_-71+51965del
ENST00000329654.8:c.-71+52582_-71+52583del	ENSP00000332116.4:n.-71+52582_-71+52583del
ENST00000341517.8:c.-71+51964_-71+51965del	ENSP00000342637.4:n.-71+51964_-71+51965del
NM_001037341.1:c.-71+52582_-71+52583del	NP_001032418.1:n.-71+52582_-71+52583del
NM_001297440.1:c.-108+52582_-108+52583del	NP_001284369.1:n.-108+52582_-108+52583del
NM_002600.3:c.-71+51964_-71+51965del	NP_002591.2:n.-71+51964_-71+51965del
NM_002600.4:c.-71+51964_-71+51965del MANE Select	NP_002591.2:n.-71+51964_-71+51965del
NM_001037341.2:c.-71+52582_-71+52583del	NP_001032418.1:n.-71+52582_-71+52583del
NM_001297440.2:c.-108+52582_-108+52583del	NP_001284369.1:n.-108+52582_-108+52583del