Canonical Allele Identifier: CA1172462458

Gene: PDE4B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.65845252_65845255delinsTTTG , CM000663.2:g.65845252_65845255delinsTTTG	GRCh38
NC_000001.10:g.66310935_66310938delinsTTTG , CM000663.1:g.66310935_66310938delinsTTTG	GRCh37
NC_000001.9:g.66083523_66083526delinsTTTG	NCBI36
NG_029038.1:g.57743_57746delinsTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341517.9:c.-71+52004_-71+52007delinsTTTG MANE Select	ENSP00000342637.4:n.-71+52004_-71+52007delinsTTTG
ENST00000329654.8:c.-71+52622_-71+52625delinsTTTG	ENSP00000332116.4:n.-71+52622_-71+52625delinsTTTG
ENST00000341517.8:c.-71+52004_-71+52007delinsTTTG	ENSP00000342637.4:n.-71+52004_-71+52007delinsTTTG
NM_001037341.1:c.-71+52622_-71+52625delinsTTTG	NP_001032418.1:n.-71+52622_-71+52625delinsTTTG
NM_001297440.1:c.-108+52622_-108+52625delinsTTTG	NP_001284369.1:n.-108+52622_-108+52625delinsTTTG
NM_002600.3:c.-71+52004_-71+52007delinsTTTG	NP_002591.2:n.-71+52004_-71+52007delinsTTTG
NM_002600.4:c.-71+52004_-71+52007delinsTTTG MANE Select	NP_002591.2:n.-71+52004_-71+52007delinsTTTG
NM_001037341.2:c.-71+52622_-71+52625delinsTTTG	NP_001032418.1:n.-71+52622_-71+52625delinsTTTG
NM_001297440.2:c.-108+52622_-108+52625delinsTTTG	NP_001284369.1:n.-108+52622_-108+52625delinsTTTG