Canonical Allele Identifier: CA798914896
Gene: PRDM8 HGNC NCBI

Linked Data

dbSNP Id: rs1192685378

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80202580del , CM000666.2:g.80202580del GRCh38
NC_000004.11:g.81123734del , CM000666.1:g.81123734del GRCh37
NC_000004.10:g.81342758del NCBI36
NG_046725.1:g.22311del

Transcript Alleles

HGVS Amino-acid Change
ENST00000415738.3:c.1118del MANE Select ENSP00000406998.2:p.Pro373ArgfsTer17
ENST00000339711.8:c.1118del ENSP00000339764.4:p.Pro373ArgfsTer17
ENST00000415738.2:c.1118del ENSP00000406998.2:p.Pro373ArgfsTer17
ENST00000504452.5:c.1118del ENSP00000423985.1:p.Pro373ArgfsTer17
ENST00000515013.5:c.1118del ENSP00000425149.1:p.Pro373ArgfsTer17
NM_001099403.1:c.1118del NP_001092873.1:p.Pro373ArgfsTer17
NM_020226.3:c.1118del NP_064611.3:p.Pro373ArgfsTer17
XM_005263144.2:c.1121del XP_005263201.1:p.Pro374ArgfsTer17
XM_005263145.2:c.1121del XP_005263202.1:p.Pro374ArgfsTer17
XM_005263146.3:c.1118del XP_005263203.1:p.Pro373ArgfsTer17
XM_011532133.1:c.1961del XP_011530435.1:p.Pro654ArgfsTer17
XM_011532134.1:c.1958del XP_011530436.1:p.Pro653ArgfsTer17
XM_011532135.1:c.1820del XP_011530437.1:p.Pro607ArgfsTer17
XM_011532136.1:c.1673del XP_011530438.1:p.Pro558ArgfsTer17
XM_011532137.1:c.1673del XP_011530439.1:p.Pro558ArgfsTer17
XM_011532138.1:c.1673del XP_011530440.1:p.Pro558ArgfsTer17
XM_011532139.1:c.1673del XP_011530441.1:p.Pro558ArgfsTer17
XM_011532140.1:c.1673del XP_011530442.1:p.Pro558ArgfsTer17
XM_011532141.1:c.1535del XP_011530443.1:p.Pro512ArgfsTer17
XM_011532142.1:c.1514del XP_011530444.1:p.Pro505ArgfsTer17
XM_005263146.4:c.1118del XP_005263203.1:p.Pro373ArgfsTer17
XM_011532133.2:c.1961del XP_011530435.1:p.Pro654ArgfsTer17
XM_011532135.2:c.1820del XP_011530437.1:p.Pro607ArgfsTer17
XM_011532140.2:c.1673del XP_011530442.1:p.Pro558ArgfsTer17
XM_011532141.3:c.1535del XP_011530443.1:p.Pro512ArgfsTer17
XM_017008468.1:c.1670del XP_016863957.1:p.Pro557ArgfsTer17
XM_017008469.1:c.1757del XP_016863958.1:p.Pro586ArgfsTer17
XM_017008470.1:c.1673del XP_016863959.1:p.Pro558ArgfsTer17
NM_001099403.2:c.1118del MANE Select NP_001092873.1:p.Pro373ArgfsTer17
NM_020226.4:c.1118del NP_064611.3:p.Pro373ArgfsTer17