Canonical Allele Identifier: CA1471293287

Gene: PRDM8

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202500G= , CM000666.2:g.80202500G=	GRCh38
NC_000004.11:g.81123654G= , CM000666.1:g.81123654G=	GRCh37
NC_000004.10:g.81342678G=	NCBI36
NG_046725.1:g.22231G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.1038G= MANE Select	ENSP00000406998.2:p.Glu346=
ENST00000339711.8:c.1038G=	ENSP00000339764.4:p.Glu346=
ENST00000415738.2:c.1038G=	ENSP00000406998.2:p.Glu346=
ENST00000504452.5:c.1038G=	ENSP00000423985.1:p.Glu346=
ENST00000515013.5:c.1038G=	ENSP00000425149.1:p.Glu346=
NM_001099403.1:c.1038G=	NP_001092873.1:p.Glu346=
NM_020226.3:c.1038G=	NP_064611.3:p.Glu346=
XM_005263144.2:c.1041G=	XP_005263201.1:p.Glu347=
XM_005263145.2:c.1041G=	XP_005263202.1:p.Glu347=
XM_005263146.3:c.1038G=	XP_005263203.1:p.Glu346=
XM_011532133.1:c.1881G=	XP_011530435.1:p.Glu627=
XM_011532134.1:c.1878G=	XP_011530436.1:p.Glu626=
XM_011532135.1:c.1740G=	XP_011530437.1:p.Glu580=
XM_011532136.1:c.1593G=	XP_011530438.1:p.Glu531=
XM_011532137.1:c.1593G=	XP_011530439.1:p.Glu531=
XM_011532138.1:c.1593G=	XP_011530440.1:p.Glu531=
XM_011532139.1:c.1593G=	XP_011530441.1:p.Glu531=
XM_011532140.1:c.1593G=	XP_011530442.1:p.Glu531=
XM_011532141.1:c.1455G=	XP_011530443.1:p.Glu485=
XM_011532142.1:c.1434G=	XP_011530444.1:p.Glu478=
XM_005263146.4:c.1038G=	XP_005263203.1:p.Glu346=
XM_011532133.2:c.1881G=	XP_011530435.1:p.Glu627=
XM_011532135.2:c.1740G=	XP_011530437.1:p.Glu580=
XM_011532140.2:c.1593G=	XP_011530442.1:p.Glu531=
XM_011532141.3:c.1455G=	XP_011530443.1:p.Glu485=
XM_017008468.1:c.1590G=	XP_016863957.1:p.Glu530=
XM_017008469.1:c.1677G=	XP_016863958.1:p.Glu559=
XM_017008470.1:c.1593G=	XP_016863959.1:p.Glu531=
NM_001099403.2:c.1038G= MANE Select	NP_001092873.1:p.Glu346=
NM_020226.4:c.1038G=	NP_064611.3:p.Glu346=