Canonical Allele Identifier: CA1172462316

Gene: PDE4B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.65845042_65845046delinsATCTG , CM000663.2:g.65845042_65845046delinsATCTG	GRCh38
NC_000001.10:g.66310725_66310729delinsATCTG , CM000663.1:g.66310725_66310729delinsATCTG	GRCh37
NC_000001.9:g.66083313_66083317delinsATCTG	NCBI36
NG_029038.1:g.57533_57537delinsATCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341517.9:c.-71+51794_-71+51798delinsATCTG MANE Select	ENSP00000342637.4:n.-71+51794_-71+51798delinsATCTG
ENST00000329654.8:c.-71+52412_-71+52416delinsATCTG	ENSP00000332116.4:n.-71+52412_-71+52416delinsATCTG
ENST00000341517.8:c.-71+51794_-71+51798delinsATCTG	ENSP00000342637.4:n.-71+51794_-71+51798delinsATCTG
NM_001037341.1:c.-71+52412_-71+52416delinsATCTG	NP_001032418.1:n.-71+52412_-71+52416delinsATCTG
NM_001297440.1:c.-108+52412_-108+52416delinsATCTG	NP_001284369.1:n.-108+52412_-108+52416delinsATCTG
NM_002600.3:c.-71+51794_-71+51798delinsATCTG	NP_002591.2:n.-71+51794_-71+51798delinsATCTG
NM_002600.4:c.-71+51794_-71+51798delinsATCTG MANE Select	NP_002591.2:n.-71+51794_-71+51798delinsATCTG
NM_001037341.2:c.-71+52412_-71+52416delinsATCTG	NP_001032418.1:n.-71+52412_-71+52416delinsATCTG
NM_001297440.2:c.-108+52412_-108+52416delinsATCTG	NP_001284369.1:n.-108+52412_-108+52416delinsATCTG