Canonical Allele Identifier: CA738007561

Gene: PDE4B

Linked Data

• dbSNP Id: rs1215140856
• MyVariant Identifiers: chr1:g.66310899_66310900insTA (hg19) ; chr1:g.65845216_65845217insTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.65845217_65845218dup , CM000663.2:g.65845217_65845218dup	GRCh38
NC_000001.10:g.66310900_66310901dup , CM000663.1:g.66310900_66310901dup	GRCh37
NC_000001.9:g.66083488_66083489dup	NCBI36
NG_029038.1:g.57708_57709dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341517.9:c.-71+51969_-71+51970dup MANE Select	ENSP00000342637.4:n.-71+51969_-71+51970dup
ENST00000329654.8:c.-71+52587_-71+52588dup	ENSP00000332116.4:n.-71+52587_-71+52588dup
ENST00000341517.8:c.-71+51969_-71+51970dup	ENSP00000342637.4:n.-71+51969_-71+51970dup
NM_001037341.1:c.-71+52587_-71+52588dup	NP_001032418.1:n.-71+52587_-71+52588dup
NM_001297440.1:c.-108+52587_-108+52588dup	NP_001284369.1:n.-108+52587_-108+52588dup
NM_002600.3:c.-71+51969_-71+51970dup	NP_002591.2:n.-71+51969_-71+51970dup
NM_002600.4:c.-71+51969_-71+51970dup MANE Select	NP_002591.2:n.-71+51969_-71+51970dup
NM_001037341.2:c.-71+52587_-71+52588dup	NP_001032418.1:n.-71+52587_-71+52588dup
NM_001297440.2:c.-108+52587_-108+52588dup	NP_001284369.1:n.-108+52587_-108+52588dup