Canonical Allele Identifier: CA440226922

Gene: PRDM8

Linked Data

• MyVariant Identifiers: chr4:g.81123615G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202461G>C , CM000666.2:g.80202461G>C	GRCh38
NC_000004.11:g.81123615G>C , CM000666.1:g.81123615G>C	GRCh37
NC_000004.10:g.81342639G>C	NCBI36
NG_046725.1:g.22192G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.999G>C MANE Select	ENSP00000406998.2:p.Arg333=
ENST00000339711.8:c.999G>C	ENSP00000339764.4:p.Arg333=
ENST00000415738.2:c.999G>C	ENSP00000406998.2:p.Arg333=
ENST00000504452.5:c.999G>C	ENSP00000423985.1:p.Arg333=
ENST00000515013.5:c.999G>C	ENSP00000425149.1:p.Arg333=
NM_001099403.1:c.999G>C	NP_001092873.1:p.Arg333=
NM_020226.3:c.999G>C	NP_064611.3:p.Arg333=
XM_005263144.2:c.1002G>C	XP_005263201.1:p.Arg334=
XM_005263145.2:c.1002G>C	XP_005263202.1:p.Arg334=
XM_005263146.3:c.999G>C	XP_005263203.1:p.Arg333=
XM_011532133.1:c.1842G>C	XP_011530435.1:p.Arg614=
XM_011532134.1:c.1839G>C	XP_011530436.1:p.Arg613=
XM_011532135.1:c.1701G>C	XP_011530437.1:p.Arg567=
XM_011532136.1:c.1554G>C	XP_011530438.1:p.Arg518=
XM_011532137.1:c.1554G>C	XP_011530439.1:p.Arg518=
XM_011532138.1:c.1554G>C	XP_011530440.1:p.Arg518=
XM_011532139.1:c.1554G>C	XP_011530441.1:p.Arg518=
XM_011532140.1:c.1554G>C	XP_011530442.1:p.Arg518=
XM_011532141.1:c.1416G>C	XP_011530443.1:p.Arg472=
XM_011532142.1:c.1395G>C	XP_011530444.1:p.Arg465=
XM_005263146.4:c.999G>C	XP_005263203.1:p.Arg333=
XM_011532133.2:c.1842G>C	XP_011530435.1:p.Arg614=
XM_011532135.2:c.1701G>C	XP_011530437.1:p.Arg567=
XM_011532140.2:c.1554G>C	XP_011530442.1:p.Arg518=
XM_011532141.3:c.1416G>C	XP_011530443.1:p.Arg472=
XM_017008468.1:c.1551G>C	XP_016863957.1:p.Arg517=
XM_017008469.1:c.1638G>C	XP_016863958.1:p.Arg546=
XM_017008470.1:c.1554G>C	XP_016863959.1:p.Arg518=
NM_001099403.2:c.999G>C MANE Select	NP_001092873.1:p.Arg333=
NM_020226.4:c.999G>C	NP_064611.3:p.Arg333=