Canonical Allele Identifier: CA2020587157
Gene: PDE3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20368732_20368734delinsAAG , CM000674.2:g.20368732_20368734delinsAAG GRCh38
NC_000012.11:g.20521666_20521668delinsAAG , CM000674.1:g.20521666_20521668delinsAAG GRCh37
NC_000012.10:g.20412933_20412935delinsAAG NCBI36
NG_030033.1:g.4488_4490delinsAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000359062.4:c.-553_-551delinsAAG MANE Select ENSP00000351957.3:n.-553_-551delinsAAG
XM_006719086.2:c.-553_-551delinsAAG XP_006719149.2:n.-553_-551delinsAAG
NM_000921.5:c.-553_-551delinsAAG MANE Select NP_000912.3:n.-553_-551delinsAAG
NM_001378407.1:c.-553_-551delinsAAG NP_001365336.1:n.-553_-551delinsAAG
NM_001378408.1:c.-1581_-1579delinsAAG NP_001365337.1:n.-1581_-1579delinsAAG