Canonical Allele Identifier: CA2762347075

Gene: PRDM8

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202170_80202171insA , CM000666.2:g.80202170_80202171insA	GRCh38
NC_000004.11:g.81123324_81123325insA , CM000666.1:g.81123324_81123325insA	GRCh37
NC_000004.10:g.81342348_81342349insA	NCBI36
NG_046725.1:g.21901_21902insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.708_709insA MANE Select	ENSP00000406998.2:p.Pro237ThrfsTer?
ENST00000339711.8:c.708_709insA	ENSP00000339764.4:p.Pro237ThrfsTer?
ENST00000415738.2:c.708_709insA	ENSP00000406998.2:p.Pro237ThrfsTer?
ENST00000504452.5:c.708_709insA	ENSP00000423985.1:p.Pro237ThrfsTer?
ENST00000515013.5:c.708_709insA	ENSP00000425149.1:p.Pro237ThrfsTer?
NM_001099403.1:c.708_709insA	NP_001092873.1:p.Pro237ThrfsTer?
NM_020226.3:c.708_709insA	NP_064611.3:p.Pro237ThrfsTer?
XM_005263144.2:c.711_712insA	XP_005263201.1:p.Pro238ThrfsTer?
XM_005263145.2:c.711_712insA	XP_005263202.1:p.Pro238ThrfsTer?
XM_005263146.3:c.708_709insA	XP_005263203.1:p.Pro237ThrfsTer?
XM_011532133.1:c.1551_1552insA	XP_011530435.1:p.Pro518ThrfsTer?
XM_011532134.1:c.1548_1549insA	XP_011530436.1:p.Pro517ThrfsTer?
XM_011532135.1:c.1410_1411insA	XP_011530437.1:p.Pro471ThrfsTer?
XM_011532136.1:c.1263_1264insA	XP_011530438.1:p.Pro422ThrfsTer?
XM_011532137.1:c.1263_1264insA	XP_011530439.1:p.Pro422ThrfsTer?
XM_011532138.1:c.1263_1264insA	XP_011530440.1:p.Pro422ThrfsTer?
XM_011532139.1:c.1263_1264insA	XP_011530441.1:p.Pro422ThrfsTer?
XM_011532140.1:c.1263_1264insA	XP_011530442.1:p.Pro422ThrfsTer?
XM_011532141.1:c.1125_1126insA	XP_011530443.1:p.Pro376ThrfsTer?
XM_011532142.1:c.1104_1105insA	XP_011530444.1:p.Pro369ThrfsTer?
XM_005263146.4:c.708_709insA	XP_005263203.1:p.Pro237ThrfsTer?
XM_011532133.2:c.1551_1552insA	XP_011530435.1:p.Pro518ThrfsTer?
XM_011532135.2:c.1410_1411insA	XP_011530437.1:p.Pro471ThrfsTer?
XM_011532140.2:c.1263_1264insA	XP_011530442.1:p.Pro422ThrfsTer?
XM_011532141.3:c.1125_1126insA	XP_011530443.1:p.Pro376ThrfsTer?
XM_017008468.1:c.1260_1261insA	XP_016863957.1:p.Pro421ThrfsTer?
XM_017008469.1:c.1347_1348insA	XP_016863958.1:p.Pro450ThrfsTer?
XM_017008470.1:c.1263_1264insA	XP_016863959.1:p.Pro422ThrfsTer?
NM_001099403.2:c.708_709insA MANE Select	NP_001092873.1:p.Pro237ThrfsTer?
NM_020226.4:c.708_709insA	NP_064611.3:p.Pro237ThrfsTer?