Canonical Allele Identifier: CA2740546071

Gene: PRDM8

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202463_80202464insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC , CM000666.2:g.80202463_80202464insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	GRCh38
NC_000004.11:g.81123617_81123618insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC , CM000666.1:g.81123617_81123618insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	GRCh37
NC_000004.10:g.81342641_81342642insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	NCBI36
NG_046725.1:g.22194_22195insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.1001_1002insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC MANE Select	ENSP00000406998.2:p.Arg335GlyfsTer15
ENST00000339711.8:c.1001_1002insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	ENSP00000339764.4:p.Arg335GlyfsTer15
ENST00000415738.2:c.1001_1002insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	ENSP00000406998.2:p.Arg335GlyfsTer15
ENST00000504452.5:c.1001_1002insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	ENSP00000423985.1:p.Arg335GlyfsTer15
ENST00000515013.5:c.1001_1002insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	ENSP00000425149.1:p.Arg335GlyfsTer15
NM_001099403.1:c.1001_1002insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	NP_001092873.1:p.Arg335GlyfsTer15
NM_020226.3:c.1001_1002insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	NP_064611.3:p.Arg335GlyfsTer15
XM_005263144.2:c.1004_1005insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	XP_005263201.1:p.Arg336GlyfsTer15
XM_005263145.2:c.1004_1005insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	XP_005263202.1:p.Arg336GlyfsTer15
XM_005263146.3:c.1001_1002insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	XP_005263203.1:p.Arg335GlyfsTer15
XM_011532133.1:c.1844_1845insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	XP_011530435.1:p.Arg616GlyfsTer15
XM_011532134.1:c.1841_1842insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	XP_011530436.1:p.Arg615GlyfsTer15
XM_011532135.1:c.1703_1704insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	XP_011530437.1:p.Arg569GlyfsTer15
XM_011532136.1:c.1556_1557insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	XP_011530438.1:p.Arg520GlyfsTer15
XM_011532137.1:c.1556_1557insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	XP_011530439.1:p.Arg520GlyfsTer15
XM_011532138.1:c.1556_1557insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	XP_011530440.1:p.Arg520GlyfsTer15
XM_011532139.1:c.1556_1557insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	XP_011530441.1:p.Arg520GlyfsTer15
XM_011532140.1:c.1556_1557insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	XP_011530442.1:p.Arg520GlyfsTer15
XM_011532141.1:c.1418_1419insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	XP_011530443.1:p.Arg474GlyfsTer15
XM_011532142.1:c.1397_1398insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	XP_011530444.1:p.Arg467GlyfsTer15
XM_005263146.4:c.1001_1002insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	XP_005263203.1:p.Arg335GlyfsTer15
XM_011532133.2:c.1844_1845insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	XP_011530435.1:p.Arg616GlyfsTer15
XM_011532135.2:c.1703_1704insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	XP_011530437.1:p.Arg569GlyfsTer15
XM_011532140.2:c.1556_1557insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	XP_011530442.1:p.Arg520GlyfsTer15
XM_011532141.3:c.1418_1419insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	XP_011530443.1:p.Arg474GlyfsTer15
XM_017008468.1:c.1553_1554insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	XP_016863957.1:p.Arg519GlyfsTer15
XM_017008469.1:c.1640_1641insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	XP_016863958.1:p.Arg548GlyfsTer15
XM_017008470.1:c.1556_1557insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	XP_016863959.1:p.Arg520GlyfsTer15
NM_001099403.2:c.1001_1002insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC MANE Select	NP_001092873.1:p.Arg335GlyfsTer15
NM_020226.4:c.1001_1002insGGGGGGGGGGGGGGGGGGGCCCCCCCCCCCCCCCC	NP_064611.3:p.Arg335GlyfsTer15