Canonical Allele Identifier: CA1471293453

Gene: PRDM8

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202576_80202579delinsGCGC , CM000666.2:g.80202576_80202579delinsGCGC	GRCh38
NC_000004.11:g.81123730_81123733delinsGCGC , CM000666.1:g.81123730_81123733delinsGCGC	GRCh37
NC_000004.10:g.81342754_81342757delinsGCGC	NCBI36
NG_046725.1:g.22307_22310delinsGCGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.1114_1117delinsGCGC MANE Select	ENSP00000406998.2:p.Ala372=
ENST00000339711.8:c.1114_1117delinsGCGC	ENSP00000339764.4:p.Ala372=
ENST00000415738.2:c.1114_1117delinsGCGC	ENSP00000406998.2:p.Ala372=
ENST00000504452.5:c.1114_1117delinsGCGC	ENSP00000423985.1:p.Ala372=
ENST00000515013.5:c.1114_1117delinsGCGC	ENSP00000425149.1:p.Ala372=
NM_001099403.1:c.1114_1117delinsGCGC	NP_001092873.1:p.Ala372=
NM_020226.3:c.1114_1117delinsGCGC	NP_064611.3:p.Ala372=
XM_005263144.2:c.1117_1120delinsGCGC	XP_005263201.1:p.Ala373=
XM_005263145.2:c.1117_1120delinsGCGC	XP_005263202.1:p.Ala373=
XM_005263146.3:c.1114_1117delinsGCGC	XP_005263203.1:p.Ala372=
XM_011532133.1:c.1957_1960delinsGCGC	XP_011530435.1:p.Ala653=
XM_011532134.1:c.1954_1957delinsGCGC	XP_011530436.1:p.Ala652=
XM_011532135.1:c.1816_1819delinsGCGC	XP_011530437.1:p.Ala606=
XM_011532136.1:c.1669_1672delinsGCGC	XP_011530438.1:p.Ala557=
XM_011532137.1:c.1669_1672delinsGCGC	XP_011530439.1:p.Ala557=
XM_011532138.1:c.1669_1672delinsGCGC	XP_011530440.1:p.Ala557=
XM_011532139.1:c.1669_1672delinsGCGC	XP_011530441.1:p.Ala557=
XM_011532140.1:c.1669_1672delinsGCGC	XP_011530442.1:p.Ala557=
XM_011532141.1:c.1531_1534delinsGCGC	XP_011530443.1:p.Ala511=
XM_011532142.1:c.1510_1513delinsGCGC	XP_011530444.1:p.Ala504=
XM_005263146.4:c.1114_1117delinsGCGC	XP_005263203.1:p.Ala372=
XM_011532133.2:c.1957_1960delinsGCGC	XP_011530435.1:p.Ala653=
XM_011532135.2:c.1816_1819delinsGCGC	XP_011530437.1:p.Ala606=
XM_011532140.2:c.1669_1672delinsGCGC	XP_011530442.1:p.Ala557=
XM_011532141.3:c.1531_1534delinsGCGC	XP_011530443.1:p.Ala511=
XM_017008468.1:c.1666_1669delinsGCGC	XP_016863957.1:p.Ala556=
XM_017008469.1:c.1753_1756delinsGCGC	XP_016863958.1:p.Ala585=
XM_017008470.1:c.1669_1672delinsGCGC	XP_016863959.1:p.Ala557=
NM_001099403.2:c.1114_1117delinsGCGC MANE Select	NP_001092873.1:p.Ala372=
NM_020226.4:c.1114_1117delinsGCGC	NP_064611.3:p.Ala372=