Canonical Allele Identifier: CA1139769839

Gene: PRDM8

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202463_80202464insGGGGGGGGGGGGGGGGGGG , CM000666.2:g.80202463_80202464insGGGGGGGGGGGGGGGGGGG	GRCh38
NC_000004.11:g.81123617_81123618insGGGGGGGGGGGGGGGGGGG , CM000666.1:g.81123617_81123618insGGGGGGGGGGGGGGGGGGG	GRCh37
NC_000004.10:g.81342641_81342642insGGGGGGGGGGGGGGGGGGG	NCBI36
NG_046725.1:g.22194_22195insGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.1001_1002insGGGGGGGGGGGGGGGGGGG MANE Select	ENSP00000406998.2:p.Arg335GlyfsTer?
ENST00000339711.8:c.1001_1002insGGGGGGGGGGGGGGGGGGG	ENSP00000339764.4:p.Arg335GlyfsTer?
ENST00000415738.2:c.1001_1002insGGGGGGGGGGGGGGGGGGG	ENSP00000406998.2:p.Arg335GlyfsTer?
ENST00000504452.5:c.1001_1002insGGGGGGGGGGGGGGGGGGG	ENSP00000423985.1:p.Arg335GlyfsTer?
ENST00000515013.5:c.1001_1002insGGGGGGGGGGGGGGGGGGG	ENSP00000425149.1:p.Arg335GlyfsTer?
NM_001099403.1:c.1001_1002insGGGGGGGGGGGGGGGGGGG	NP_001092873.1:p.Arg335GlyfsTer?
NM_020226.3:c.1001_1002insGGGGGGGGGGGGGGGGGGG	NP_064611.3:p.Arg335GlyfsTer?
XM_005263144.2:c.1004_1005insGGGGGGGGGGGGGGGGGGG	XP_005263201.1:p.Arg336GlyfsTer?
XM_005263145.2:c.1004_1005insGGGGGGGGGGGGGGGGGGG	XP_005263202.1:p.Arg336GlyfsTer?
XM_005263146.3:c.1001_1002insGGGGGGGGGGGGGGGGGGG	XP_005263203.1:p.Arg335GlyfsTer?
XM_011532133.1:c.1844_1845insGGGGGGGGGGGGGGGGGGG	XP_011530435.1:p.Arg616GlyfsTer?
XM_011532134.1:c.1841_1842insGGGGGGGGGGGGGGGGGGG	XP_011530436.1:p.Arg615GlyfsTer?
XM_011532135.1:c.1703_1704insGGGGGGGGGGGGGGGGGGG	XP_011530437.1:p.Arg569GlyfsTer?
XM_011532136.1:c.1556_1557insGGGGGGGGGGGGGGGGGGG	XP_011530438.1:p.Arg520GlyfsTer?
XM_011532137.1:c.1556_1557insGGGGGGGGGGGGGGGGGGG	XP_011530439.1:p.Arg520GlyfsTer?
XM_011532138.1:c.1556_1557insGGGGGGGGGGGGGGGGGGG	XP_011530440.1:p.Arg520GlyfsTer?
XM_011532139.1:c.1556_1557insGGGGGGGGGGGGGGGGGGG	XP_011530441.1:p.Arg520GlyfsTer?
XM_011532140.1:c.1556_1557insGGGGGGGGGGGGGGGGGGG	XP_011530442.1:p.Arg520GlyfsTer?
XM_011532141.1:c.1418_1419insGGGGGGGGGGGGGGGGGGG	XP_011530443.1:p.Arg474GlyfsTer?
XM_011532142.1:c.1397_1398insGGGGGGGGGGGGGGGGGGG	XP_011530444.1:p.Arg467GlyfsTer?
XM_005263146.4:c.1001_1002insGGGGGGGGGGGGGGGGGGG	XP_005263203.1:p.Arg335GlyfsTer?
XM_011532133.2:c.1844_1845insGGGGGGGGGGGGGGGGGGG	XP_011530435.1:p.Arg616GlyfsTer?
XM_011532135.2:c.1703_1704insGGGGGGGGGGGGGGGGGGG	XP_011530437.1:p.Arg569GlyfsTer?
XM_011532140.2:c.1556_1557insGGGGGGGGGGGGGGGGGGG	XP_011530442.1:p.Arg520GlyfsTer?
XM_011532141.3:c.1418_1419insGGGGGGGGGGGGGGGGGGG	XP_011530443.1:p.Arg474GlyfsTer?
XM_017008468.1:c.1553_1554insGGGGGGGGGGGGGGGGGGG	XP_016863957.1:p.Arg519GlyfsTer?
XM_017008469.1:c.1640_1641insGGGGGGGGGGGGGGGGGGG	XP_016863958.1:p.Arg548GlyfsTer?
XM_017008470.1:c.1556_1557insGGGGGGGGGGGGGGGGGGG	XP_016863959.1:p.Arg520GlyfsTer?
NM_001099403.2:c.1001_1002insGGGGGGGGGGGGGGGGGGG MANE Select	NP_001092873.1:p.Arg335GlyfsTer?
NM_020226.4:c.1001_1002insGGGGGGGGGGGGGGGGGGG	NP_064611.3:p.Arg335GlyfsTer?