Canonical Allele Identifier: CA1471292462

Gene: PRDM8

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202173_80202174delinsAT , CM000666.2:g.80202173_80202174delinsAT	GRCh38
NC_000004.11:g.81123327_81123328delinsAT , CM000666.1:g.81123327_81123328delinsAT	GRCh37
NC_000004.10:g.81342351_81342352delinsAT	NCBI36
NG_046725.1:g.21904_21905delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.711_712delinsAT MANE Select	ENSP00000406998.2:p.Pro237=
ENST00000339711.8:c.711_712delinsAT	ENSP00000339764.4:p.Pro237=
ENST00000415738.2:c.711_712delinsAT	ENSP00000406998.2:p.Pro237=
ENST00000504452.5:c.711_712delinsAT	ENSP00000423985.1:p.Pro237=
ENST00000515013.5:c.711_712delinsAT	ENSP00000425149.1:p.Pro237=
NM_001099403.1:c.711_712delinsAT	NP_001092873.1:p.Pro237=
NM_020226.3:c.711_712delinsAT	NP_064611.3:p.Pro237=
XM_005263144.2:c.714_715delinsAT	XP_005263201.1:p.Pro238=
XM_005263145.2:c.714_715delinsAT	XP_005263202.1:p.Pro238=
XM_005263146.3:c.711_712delinsAT	XP_005263203.1:p.Pro237=
XM_011532133.1:c.1554_1555delinsAT	XP_011530435.1:p.Pro518=
XM_011532134.1:c.1551_1552delinsAT	XP_011530436.1:p.Pro517=
XM_011532135.1:c.1413_1414delinsAT	XP_011530437.1:p.Pro471=
XM_011532136.1:c.1266_1267delinsAT	XP_011530438.1:p.Pro422=
XM_011532137.1:c.1266_1267delinsAT	XP_011530439.1:p.Pro422=
XM_011532138.1:c.1266_1267delinsAT	XP_011530440.1:p.Pro422=
XM_011532139.1:c.1266_1267delinsAT	XP_011530441.1:p.Pro422=
XM_011532140.1:c.1266_1267delinsAT	XP_011530442.1:p.Pro422=
XM_011532141.1:c.1128_1129delinsAT	XP_011530443.1:p.Pro376=
XM_011532142.1:c.1107_1108delinsAT	XP_011530444.1:p.Pro369=
XM_005263146.4:c.711_712delinsAT	XP_005263203.1:p.Pro237=
XM_011532133.2:c.1554_1555delinsAT	XP_011530435.1:p.Pro518=
XM_011532135.2:c.1413_1414delinsAT	XP_011530437.1:p.Pro471=
XM_011532140.2:c.1266_1267delinsAT	XP_011530442.1:p.Pro422=
XM_011532141.3:c.1128_1129delinsAT	XP_011530443.1:p.Pro376=
XM_017008468.1:c.1263_1264delinsAT	XP_016863957.1:p.Pro421=
XM_017008469.1:c.1350_1351delinsAT	XP_016863958.1:p.Pro450=
XM_017008470.1:c.1266_1267delinsAT	XP_016863959.1:p.Pro422=
NM_001099403.2:c.711_712delinsAT MANE Select	NP_001092873.1:p.Pro237=
NM_020226.4:c.711_712delinsAT	NP_064611.3:p.Pro237=