Canonical Allele Identifier: CA1471293001

Gene: PRDM8

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202382C= , CM000666.2:g.80202382C=	GRCh38
NC_000004.11:g.81123536C= , CM000666.1:g.81123536C=	GRCh37
NC_000004.10:g.81342560C=	NCBI36
NG_046725.1:g.22113C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.920C= MANE Select	ENSP00000406998.2:p.Thr307=
ENST00000339711.8:c.920C=	ENSP00000339764.4:p.Thr307=
ENST00000415738.2:c.920C=	ENSP00000406998.2:p.Thr307=
ENST00000504452.5:c.920C=	ENSP00000423985.1:p.Thr307=
ENST00000515013.5:c.920C=	ENSP00000425149.1:p.Thr307=
NM_001099403.1:c.920C=	NP_001092873.1:p.Thr307=
NM_020226.3:c.920C=	NP_064611.3:p.Thr307=
XM_005263144.2:c.923C=	XP_005263201.1:p.Thr308=
XM_005263145.2:c.923C=	XP_005263202.1:p.Thr308=
XM_005263146.3:c.920C=	XP_005263203.1:p.Thr307=
XM_011532133.1:c.1763C=	XP_011530435.1:p.Thr588=
XM_011532134.1:c.1760C=	XP_011530436.1:p.Thr587=
XM_011532135.1:c.1622C=	XP_011530437.1:p.Thr541=
XM_011532136.1:c.1475C=	XP_011530438.1:p.Thr492=
XM_011532137.1:c.1475C=	XP_011530439.1:p.Thr492=
XM_011532138.1:c.1475C=	XP_011530440.1:p.Thr492=
XM_011532139.1:c.1475C=	XP_011530441.1:p.Thr492=
XM_011532140.1:c.1475C=	XP_011530442.1:p.Thr492=
XM_011532141.1:c.1337C=	XP_011530443.1:p.Thr446=
XM_011532142.1:c.1316C=	XP_011530444.1:p.Thr439=
XM_005263146.4:c.920C=	XP_005263203.1:p.Thr307=
XM_011532133.2:c.1763C=	XP_011530435.1:p.Thr588=
XM_011532135.2:c.1622C=	XP_011530437.1:p.Thr541=
XM_011532140.2:c.1475C=	XP_011530442.1:p.Thr492=
XM_011532141.3:c.1337C=	XP_011530443.1:p.Thr446=
XM_017008468.1:c.1472C=	XP_016863957.1:p.Thr491=
XM_017008469.1:c.1559C=	XP_016863958.1:p.Thr520=
XM_017008470.1:c.1475C=	XP_016863959.1:p.Thr492=
NM_001099403.2:c.920C= MANE Select	NP_001092873.1:p.Thr307=
NM_020226.4:c.920C=	NP_064611.3:p.Thr307=