Canonical Allele Identifier: CA1471292452

Gene: PRDM8

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202171C= , CM000666.2:g.80202171C=	GRCh38
NC_000004.11:g.81123325C= , CM000666.1:g.81123325C=	GRCh37
NC_000004.10:g.81342349C=	NCBI36
NG_046725.1:g.21902C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.709C= MANE Select	ENSP00000406998.2:p.Pro237=
ENST00000339711.8:c.709C=	ENSP00000339764.4:p.Pro237=
ENST00000415738.2:c.709C=	ENSP00000406998.2:p.Pro237=
ENST00000504452.5:c.709C=	ENSP00000423985.1:p.Pro237=
ENST00000515013.5:c.709C=	ENSP00000425149.1:p.Pro237=
NM_001099403.1:c.709C=	NP_001092873.1:p.Pro237=
NM_020226.3:c.709C=	NP_064611.3:p.Pro237=
XM_005263144.2:c.712C=	XP_005263201.1:p.Pro238=
XM_005263145.2:c.712C=	XP_005263202.1:p.Pro238=
XM_005263146.3:c.709C=	XP_005263203.1:p.Pro237=
XM_011532133.1:c.1552C=	XP_011530435.1:p.Pro518=
XM_011532134.1:c.1549C=	XP_011530436.1:p.Pro517=
XM_011532135.1:c.1411C=	XP_011530437.1:p.Pro471=
XM_011532136.1:c.1264C=	XP_011530438.1:p.Pro422=
XM_011532137.1:c.1264C=	XP_011530439.1:p.Pro422=
XM_011532138.1:c.1264C=	XP_011530440.1:p.Pro422=
XM_011532139.1:c.1264C=	XP_011530441.1:p.Pro422=
XM_011532140.1:c.1264C=	XP_011530442.1:p.Pro422=
XM_011532141.1:c.1126C=	XP_011530443.1:p.Pro376=
XM_011532142.1:c.1105C=	XP_011530444.1:p.Pro369=
XM_005263146.4:c.709C=	XP_005263203.1:p.Pro237=
XM_011532133.2:c.1552C=	XP_011530435.1:p.Pro518=
XM_011532135.2:c.1411C=	XP_011530437.1:p.Pro471=
XM_011532140.2:c.1264C=	XP_011530442.1:p.Pro422=
XM_011532141.3:c.1126C=	XP_011530443.1:p.Pro376=
XM_017008468.1:c.1261C=	XP_016863957.1:p.Pro421=
XM_017008469.1:c.1348C=	XP_016863958.1:p.Pro450=
XM_017008470.1:c.1264C=	XP_016863959.1:p.Pro422=
NM_001099403.2:c.709C= MANE Select	NP_001092873.1:p.Pro237=
NM_020226.4:c.709C=	NP_064611.3:p.Pro237=