Canonical Allele Identifier: CA2671177959

Gene: PRDM8

Linked Data

• gnomAD v4: 4-80202449-GGTAGGGGGCCGGGGCCGCTTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202454_80202474del , CM000666.2:g.80202454_80202474del	GRCh38
NC_000004.11:g.81123608_81123628del , CM000666.1:g.81123608_81123628del	GRCh37
NC_000004.10:g.81342632_81342652del	NCBI36
NG_046725.1:g.22185_22205del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.992_1012del MANE Select	ENSP00000406998.2:p.Gly331_Val337del
ENST00000339711.8:c.992_1012del	ENSP00000339764.4:p.Gly331_Val337del
ENST00000415738.2:c.992_1012del	ENSP00000406998.2:p.Gly331_Val337del
ENST00000504452.5:c.992_1012del	ENSP00000423985.1:p.Gly331_Val337del
ENST00000515013.5:c.992_1012del	ENSP00000425149.1:p.Gly331_Val337del
NM_001099403.1:c.992_1012del	NP_001092873.1:p.Gly331_Val337del
NM_020226.3:c.992_1012del	NP_064611.3:p.Gly331_Val337del
XM_005263144.2:c.995_1015del	XP_005263201.1:p.Gly332_Val338del
XM_005263145.2:c.995_1015del	XP_005263202.1:p.Gly332_Val338del
XM_005263146.3:c.992_1012del	XP_005263203.1:p.Gly331_Val337del
XM_011532133.1:c.1835_1855del	XP_011530435.1:p.Gly612_Val618del
XM_011532134.1:c.1832_1852del	XP_011530436.1:p.Gly611_Val617del
XM_011532135.1:c.1694_1714del	XP_011530437.1:p.Gly565_Val571del
XM_011532136.1:c.1547_1567del	XP_011530438.1:p.Gly516_Val522del
XM_011532137.1:c.1547_1567del	XP_011530439.1:p.Gly516_Val522del
XM_011532138.1:c.1547_1567del	XP_011530440.1:p.Gly516_Val522del
XM_011532139.1:c.1547_1567del	XP_011530441.1:p.Gly516_Val522del
XM_011532140.1:c.1547_1567del	XP_011530442.1:p.Gly516_Val522del
XM_011532141.1:c.1409_1429del	XP_011530443.1:p.Gly470_Val476del
XM_011532142.1:c.1388_1408del	XP_011530444.1:p.Gly463_Val469del
XM_005263146.4:c.992_1012del	XP_005263203.1:p.Gly331_Val337del
XM_011532133.2:c.1835_1855del	XP_011530435.1:p.Gly612_Val618del
XM_011532135.2:c.1694_1714del	XP_011530437.1:p.Gly565_Val571del
XM_011532140.2:c.1547_1567del	XP_011530442.1:p.Gly516_Val522del
XM_011532141.3:c.1409_1429del	XP_011530443.1:p.Gly470_Val476del
XM_017008468.1:c.1544_1564del	XP_016863957.1:p.Gly515_Val521del
XM_017008469.1:c.1631_1651del	XP_016863958.1:p.Gly544_Val550del
XM_017008470.1:c.1547_1567del	XP_016863959.1:p.Gly516_Val522del
NM_001099403.2:c.992_1012del MANE Select	NP_001092873.1:p.Gly331_Val337del
NM_020226.4:c.992_1012del	NP_064611.3:p.Gly331_Val337del