Canonical Allele Identifier: CA2563058736

Gene: PRDM8

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202517_80202518insAGGTCCTCCTTGGAGGCCGGGAGGG , CM000666.2:g.80202517_80202518insAGGTCCTCCTTGGAGGCCGGGAGGG	GRCh38
NC_000004.11:g.81123671_81123672insAGGTCCTCCTTGGAGGCCGGGAGGG , CM000666.1:g.81123671_81123672insAGGTCCTCCTTGGAGGCCGGGAGGG	GRCh37
NC_000004.10:g.81342695_81342696insAGGTCCTCCTTGGAGGCCGGGAGGG	NCBI36
NG_046725.1:g.22248_22249insAGGTCCTCCTTGGAGGCCGGGAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.1055_1056insAGGTCCTCCTTGGAGGCCGGGAGGG MANE Select	ENSP00000406998.2:p.Gln353GlyfsTer?
ENST00000339711.8:c.1055_1056insAGGTCCTCCTTGGAGGCCGGGAGGG	ENSP00000339764.4:p.Gln353GlyfsTer?
ENST00000415738.2:c.1055_1056insAGGTCCTCCTTGGAGGCCGGGAGGG	ENSP00000406998.2:p.Gln353GlyfsTer?
ENST00000504452.5:c.1055_1056insAGGTCCTCCTTGGAGGCCGGGAGGG	ENSP00000423985.1:p.Gln353GlyfsTer?
ENST00000515013.5:c.1055_1056insAGGTCCTCCTTGGAGGCCGGGAGGG	ENSP00000425149.1:p.Gln353GlyfsTer?
NM_001099403.1:c.1055_1056insAGGTCCTCCTTGGAGGCCGGGAGGG	NP_001092873.1:p.Gln353GlyfsTer?
NM_020226.3:c.1055_1056insAGGTCCTCCTTGGAGGCCGGGAGGG	NP_064611.3:p.Gln353GlyfsTer?
XM_005263144.2:c.1058_1059insAGGTCCTCCTTGGAGGCCGGGAGGG	XP_005263201.1:p.Gln354GlyfsTer?
XM_005263145.2:c.1058_1059insAGGTCCTCCTTGGAGGCCGGGAGGG	XP_005263202.1:p.Gln354GlyfsTer?
XM_005263146.3:c.1055_1056insAGGTCCTCCTTGGAGGCCGGGAGGG	XP_005263203.1:p.Gln353GlyfsTer?
XM_011532133.1:c.1898_1899insAGGTCCTCCTTGGAGGCCGGGAGGG	XP_011530435.1:p.Gln634GlyfsTer?
XM_011532134.1:c.1895_1896insAGGTCCTCCTTGGAGGCCGGGAGGG	XP_011530436.1:p.Gln633GlyfsTer?
XM_011532135.1:c.1757_1758insAGGTCCTCCTTGGAGGCCGGGAGGG	XP_011530437.1:p.Gln587GlyfsTer?
XM_011532136.1:c.1610_1611insAGGTCCTCCTTGGAGGCCGGGAGGG	XP_011530438.1:p.Gln538GlyfsTer?
XM_011532137.1:c.1610_1611insAGGTCCTCCTTGGAGGCCGGGAGGG	XP_011530439.1:p.Gln538GlyfsTer?
XM_011532138.1:c.1610_1611insAGGTCCTCCTTGGAGGCCGGGAGGG	XP_011530440.1:p.Gln538GlyfsTer?
XM_011532139.1:c.1610_1611insAGGTCCTCCTTGGAGGCCGGGAGGG	XP_011530441.1:p.Gln538GlyfsTer?
XM_011532140.1:c.1610_1611insAGGTCCTCCTTGGAGGCCGGGAGGG	XP_011530442.1:p.Gln538GlyfsTer?
XM_011532141.1:c.1472_1473insAGGTCCTCCTTGGAGGCCGGGAGGG	XP_011530443.1:p.Gln492GlyfsTer?
XM_011532142.1:c.1451_1452insAGGTCCTCCTTGGAGGCCGGGAGGG	XP_011530444.1:p.Gln485GlyfsTer?
XM_005263146.4:c.1055_1056insAGGTCCTCCTTGGAGGCCGGGAGGG	XP_005263203.1:p.Gln353GlyfsTer?
XM_011532133.2:c.1898_1899insAGGTCCTCCTTGGAGGCCGGGAGGG	XP_011530435.1:p.Gln634GlyfsTer?
XM_011532135.2:c.1757_1758insAGGTCCTCCTTGGAGGCCGGGAGGG	XP_011530437.1:p.Gln587GlyfsTer?
XM_011532140.2:c.1610_1611insAGGTCCTCCTTGGAGGCCGGGAGGG	XP_011530442.1:p.Gln538GlyfsTer?
XM_011532141.3:c.1472_1473insAGGTCCTCCTTGGAGGCCGGGAGGG	XP_011530443.1:p.Gln492GlyfsTer?
XM_017008468.1:c.1607_1608insAGGTCCTCCTTGGAGGCCGGGAGGG	XP_016863957.1:p.Gln537GlyfsTer?
XM_017008469.1:c.1694_1695insAGGTCCTCCTTGGAGGCCGGGAGGG	XP_016863958.1:p.Gln566GlyfsTer?
XM_017008470.1:c.1610_1611insAGGTCCTCCTTGGAGGCCGGGAGGG	XP_016863959.1:p.Gln538GlyfsTer?
NM_001099403.2:c.1055_1056insAGGTCCTCCTTGGAGGCCGGGAGGG MANE Select	NP_001092873.1:p.Gln353GlyfsTer?
NM_020226.4:c.1055_1056insAGGTCCTCCTTGGAGGCCGGGAGGG	NP_064611.3:p.Gln353GlyfsTer?