Canonical Allele Identifier: CA1471293044

Gene: PRDM8

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202404G= , CM000666.2:g.80202404G=	GRCh38
NC_000004.11:g.81123558G= , CM000666.1:g.81123558G=	GRCh37
NC_000004.10:g.81342582G=	NCBI36
NG_046725.1:g.22135G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.942G= MANE Select	ENSP00000406998.2:p.Arg314=
ENST00000339711.8:c.942G=	ENSP00000339764.4:p.Arg314=
ENST00000415738.2:c.942G=	ENSP00000406998.2:p.Arg314=
ENST00000504452.5:c.942G=	ENSP00000423985.1:p.Arg314=
ENST00000515013.5:c.942G=	ENSP00000425149.1:p.Arg314=
NM_001099403.1:c.942G=	NP_001092873.1:p.Arg314=
NM_020226.3:c.942G=	NP_064611.3:p.Arg314=
XM_005263144.2:c.945G=	XP_005263201.1:p.Arg315=
XM_005263145.2:c.945G=	XP_005263202.1:p.Arg315=
XM_005263146.3:c.942G=	XP_005263203.1:p.Arg314=
XM_011532133.1:c.1785G=	XP_011530435.1:p.Arg595=
XM_011532134.1:c.1782G=	XP_011530436.1:p.Arg594=
XM_011532135.1:c.1644G=	XP_011530437.1:p.Arg548=
XM_011532136.1:c.1497G=	XP_011530438.1:p.Arg499=
XM_011532137.1:c.1497G=	XP_011530439.1:p.Arg499=
XM_011532138.1:c.1497G=	XP_011530440.1:p.Arg499=
XM_011532139.1:c.1497G=	XP_011530441.1:p.Arg499=
XM_011532140.1:c.1497G=	XP_011530442.1:p.Arg499=
XM_011532141.1:c.1359G=	XP_011530443.1:p.Arg453=
XM_011532142.1:c.1338G=	XP_011530444.1:p.Arg446=
XM_005263146.4:c.942G=	XP_005263203.1:p.Arg314=
XM_011532133.2:c.1785G=	XP_011530435.1:p.Arg595=
XM_011532135.2:c.1644G=	XP_011530437.1:p.Arg548=
XM_011532140.2:c.1497G=	XP_011530442.1:p.Arg499=
XM_011532141.3:c.1359G=	XP_011530443.1:p.Arg453=
XM_017008468.1:c.1494G=	XP_016863957.1:p.Arg498=
XM_017008469.1:c.1581G=	XP_016863958.1:p.Arg527=
XM_017008470.1:c.1497G=	XP_016863959.1:p.Arg499=
NM_001099403.2:c.942G= MANE Select	NP_001092873.1:p.Arg314=
NM_020226.4:c.942G=	NP_064611.3:p.Arg314=