Canonical Allele Identifier: CA686318118
Gene: PDE3A HGNC NCBI

Linked Data

dbSNP Id: rs1463301159

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20368794_20368820del , CM000674.2:g.20368794_20368820del GRCh38
NC_000012.11:g.20521728_20521754del , CM000674.1:g.20521728_20521754del GRCh37
NC_000012.10:g.20412995_20413021del NCBI36
NG_030033.1:g.4550_4576del

Transcript Alleles

HGVS Amino-acid Change
ENST00000359062.4:c.-491_-465del MANE Select ENSP00000351957.3:n.-491_-465del
XM_006719086.2:c.-491_-465del XP_006719149.2:n.-491_-465del
NM_000921.5:c.-491_-465del MANE Select NP_000912.3:n.-491_-465del
NM_001378407.1:c.-491_-465del NP_001365336.1:n.-491_-465del
NM_001378408.1:c.-1519_-1493del NP_001365337.1:n.-1519_-1493del