Canonical Allele Identifier: CA440226891

Gene: PRDM8

Linked Data

• gnomAD v4: 4-80202258-A-C
• MyVariant Identifiers: chr4:g.81123412A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202258A>C , CM000666.2:g.80202258A>C	GRCh38
NC_000004.11:g.81123412A>C , CM000666.1:g.81123412A>C	GRCh37
NC_000004.10:g.81342436A>C	NCBI36
NG_046725.1:g.21989A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000415738.3:c.796A>C MANE Select	ENSP00000406998.2:p.Arg266=
ENST00000339711.8:c.796A>C	ENSP00000339764.4:p.Arg266=
ENST00000415738.2:c.796A>C	ENSP00000406998.2:p.Arg266=
ENST00000504452.5:c.796A>C	ENSP00000423985.1:p.Arg266=
ENST00000515013.5:c.796A>C	ENSP00000425149.1:p.Arg266=
NM_001099403.1:c.796A>C	NP_001092873.1:p.Arg266=
NM_020226.3:c.796A>C	NP_064611.3:p.Arg266=
XM_005263144.2:c.799A>C	XP_005263201.1:p.Arg267=
XM_005263145.2:c.799A>C	XP_005263202.1:p.Arg267=
XM_005263146.3:c.796A>C	XP_005263203.1:p.Arg266=
XM_011532133.1:c.1639A>C	XP_011530435.1:p.Arg547=
XM_011532134.1:c.1636A>C	XP_011530436.1:p.Arg546=
XM_011532135.1:c.1498A>C	XP_011530437.1:p.Arg500=
XM_011532136.1:c.1351A>C	XP_011530438.1:p.Arg451=
XM_011532137.1:c.1351A>C	XP_011530439.1:p.Arg451=
XM_011532138.1:c.1351A>C	XP_011530440.1:p.Arg451=
XM_011532139.1:c.1351A>C	XP_011530441.1:p.Arg451=
XM_011532140.1:c.1351A>C	XP_011530442.1:p.Arg451=
XM_011532141.1:c.1213A>C	XP_011530443.1:p.Arg405=
XM_011532142.1:c.1192A>C	XP_011530444.1:p.Arg398=
XM_005263146.4:c.796A>C	XP_005263203.1:p.Arg266=
XM_011532133.2:c.1639A>C	XP_011530435.1:p.Arg547=
XM_011532135.2:c.1498A>C	XP_011530437.1:p.Arg500=
XM_011532140.2:c.1351A>C	XP_011530442.1:p.Arg451=
XM_011532141.3:c.1213A>C	XP_011530443.1:p.Arg405=
XM_017008468.1:c.1348A>C	XP_016863957.1:p.Arg450=
XM_017008469.1:c.1435A>C	XP_016863958.1:p.Arg479=
XM_017008470.1:c.1351A>C	XP_016863959.1:p.Arg451=
NM_001099403.2:c.796A>C MANE Select	NP_001092873.1:p.Arg266=
NM_020226.4:c.796A>C	NP_064611.3:p.Arg266=