Canonical Allele Identifier: CA1139770266

Gene: PRDM8

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202479_80202480insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC , CM000666.2:g.80202479_80202480insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	GRCh38
NC_000004.11:g.81123633_81123634insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC , CM000666.1:g.81123633_81123634insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	GRCh37
NC_000004.10:g.81342657_81342658insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	NCBI36
NG_046725.1:g.22210_22211insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.1017_1018insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC MANE Select	ENSP00000406998.2:p.Pro340GlyfsTer?
ENST00000339711.8:c.1017_1018insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	ENSP00000339764.4:p.Pro340GlyfsTer?
ENST00000415738.2:c.1017_1018insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	ENSP00000406998.2:p.Pro340GlyfsTer?
ENST00000504452.5:c.1017_1018insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	ENSP00000423985.1:p.Pro340GlyfsTer?
ENST00000515013.5:c.1017_1018insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	ENSP00000425149.1:p.Pro340GlyfsTer?
NM_001099403.1:c.1017_1018insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	NP_001092873.1:p.Pro340GlyfsTer?
NM_020226.3:c.1017_1018insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	NP_064611.3:p.Pro340GlyfsTer?
XM_005263144.2:c.1020_1021insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	XP_005263201.1:p.Pro341GlyfsTer?
XM_005263145.2:c.1020_1021insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	XP_005263202.1:p.Pro341GlyfsTer?
XM_005263146.3:c.1017_1018insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	XP_005263203.1:p.Pro340GlyfsTer?
XM_011532133.1:c.1860_1861insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	XP_011530435.1:p.Pro621GlyfsTer?
XM_011532134.1:c.1857_1858insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	XP_011530436.1:p.Pro620GlyfsTer?
XM_011532135.1:c.1719_1720insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	XP_011530437.1:p.Pro574GlyfsTer?
XM_011532136.1:c.1572_1573insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	XP_011530438.1:p.Pro525GlyfsTer?
XM_011532137.1:c.1572_1573insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	XP_011530439.1:p.Pro525GlyfsTer?
XM_011532138.1:c.1572_1573insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	XP_011530440.1:p.Pro525GlyfsTer?
XM_011532139.1:c.1572_1573insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	XP_011530441.1:p.Pro525GlyfsTer?
XM_011532140.1:c.1572_1573insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	XP_011530442.1:p.Pro525GlyfsTer?
XM_011532141.1:c.1434_1435insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	XP_011530443.1:p.Pro479GlyfsTer?
XM_011532142.1:c.1413_1414insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	XP_011530444.1:p.Pro472GlyfsTer?
XM_005263146.4:c.1017_1018insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	XP_005263203.1:p.Pro340GlyfsTer?
XM_011532133.2:c.1860_1861insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	XP_011530435.1:p.Pro621GlyfsTer?
XM_011532135.2:c.1719_1720insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	XP_011530437.1:p.Pro574GlyfsTer?
XM_011532140.2:c.1572_1573insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	XP_011530442.1:p.Pro525GlyfsTer?
XM_011532141.3:c.1434_1435insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	XP_011530443.1:p.Pro479GlyfsTer?
XM_017008468.1:c.1569_1570insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	XP_016863957.1:p.Pro524GlyfsTer?
XM_017008469.1:c.1656_1657insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	XP_016863958.1:p.Pro553GlyfsTer?
XM_017008470.1:c.1572_1573insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	XP_016863959.1:p.Pro525GlyfsTer?
NM_001099403.2:c.1017_1018insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC MANE Select	NP_001092873.1:p.Pro340GlyfsTer?
NM_020226.4:c.1017_1018insGGGGGGGGGGGGGGGGGGGGGGGGTTGGGTCCCCCCC	NP_064611.3:p.Pro340GlyfsTer?