Canonical Allele Identifier: CA357396928
Gene: PRDM8 HGNC NCBI

Linked Data

dbSNP Id: rs904039995
gnomAD v4: 4-80202391-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80202391G>A , CM000666.2:g.80202391G>A GRCh38
NC_000004.11:g.81123545G>A , CM000666.1:g.81123545G>A GRCh37
NC_000004.10:g.81342569G>A NCBI36
NG_046725.1:g.22122G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000415738.3:c.929G>A MANE Select ENSP00000406998.2:p.Gly310Asp
ENST00000339711.8:c.929G>A ENSP00000339764.4:p.Gly310Asp
ENST00000415738.2:c.929G>A ENSP00000406998.2:p.Gly310Asp
ENST00000504452.5:c.929G>A ENSP00000423985.1:p.Gly310Asp
ENST00000515013.5:c.929G>A ENSP00000425149.1:p.Gly310Asp
NM_001099403.1:c.929G>A NP_001092873.1:p.Gly310Asp
NM_020226.3:c.929G>A NP_064611.3:p.Gly310Asp
XM_005263144.2:c.932G>A XP_005263201.1:p.Gly311Asp
XM_005263145.2:c.932G>A XP_005263202.1:p.Gly311Asp
XM_005263146.3:c.929G>A XP_005263203.1:p.Gly310Asp
XM_011532133.1:c.1772G>A XP_011530435.1:p.Gly591Asp
XM_011532134.1:c.1769G>A XP_011530436.1:p.Gly590Asp
XM_011532135.1:c.1631G>A XP_011530437.1:p.Gly544Asp
XM_011532136.1:c.1484G>A XP_011530438.1:p.Gly495Asp
XM_011532137.1:c.1484G>A XP_011530439.1:p.Gly495Asp
XM_011532138.1:c.1484G>A XP_011530440.1:p.Gly495Asp
XM_011532139.1:c.1484G>A XP_011530441.1:p.Gly495Asp
XM_011532140.1:c.1484G>A XP_011530442.1:p.Gly495Asp
XM_011532141.1:c.1346G>A XP_011530443.1:p.Gly449Asp
XM_011532142.1:c.1325G>A XP_011530444.1:p.Gly442Asp
XM_005263146.4:c.929G>A XP_005263203.1:p.Gly310Asp
XM_011532133.2:c.1772G>A XP_011530435.1:p.Gly591Asp
XM_011532135.2:c.1631G>A XP_011530437.1:p.Gly544Asp
XM_011532140.2:c.1484G>A XP_011530442.1:p.Gly495Asp
XM_011532141.3:c.1346G>A XP_011530443.1:p.Gly449Asp
XM_017008468.1:c.1481G>A XP_016863957.1:p.Gly494Asp
XM_017008469.1:c.1568G>A XP_016863958.1:p.Gly523Asp
XM_017008470.1:c.1484G>A XP_016863959.1:p.Gly495Asp
NM_001099403.2:c.929G>A MANE Select NP_001092873.1:p.Gly310Asp
NM_020226.4:c.929G>A NP_064611.3:p.Gly310Asp