Canonical Allele Identifier: CA2982320

Gene: PRDM8

Linked Data

• ClinVar Variation Id: 1046471
• ClinVar RCV Id: RCV001351035
• dbSNP Id: rs750455114
• ExAC: 4:81123358 G / A
• gnomAD v2: 4-81123358-G-A
• gnomAD v4: 4-80202204-G-A
• MyVariant Identifiers: chr4:g.81123358G>A (hg19) ; chr4:g.80202204G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202204G>A , CM000666.2:g.80202204G>A	GRCh38
NC_000004.11:g.81123358G>A , CM000666.1:g.81123358G>A	GRCh37
NC_000004.10:g.81342382G>A	NCBI36
NG_046725.1:g.21935G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.742G>A MANE Select	ENSP00000406998.2:p.Ala248Thr
ENST00000339711.8:c.742G>A	ENSP00000339764.4:p.Ala248Thr
ENST00000415738.2:c.742G>A	ENSP00000406998.2:p.Ala248Thr
ENST00000504452.5:c.742G>A	ENSP00000423985.1:p.Ala248Thr
ENST00000515013.5:c.742G>A	ENSP00000425149.1:p.Ala248Thr
NM_001099403.1:c.742G>A	NP_001092873.1:p.Ala248Thr
NM_020226.3:c.742G>A	NP_064611.3:p.Ala248Thr
XM_005263144.2:c.745G>A	XP_005263201.1:p.Ala249Thr
XM_005263145.2:c.745G>A	XP_005263202.1:p.Ala249Thr
XM_005263146.3:c.742G>A	XP_005263203.1:p.Ala248Thr
XM_011532133.1:c.1585G>A	XP_011530435.1:p.Ala529Thr
XM_011532134.1:c.1582G>A	XP_011530436.1:p.Ala528Thr
XM_011532135.1:c.1444G>A	XP_011530437.1:p.Ala482Thr
XM_011532136.1:c.1297G>A	XP_011530438.1:p.Ala433Thr
XM_011532137.1:c.1297G>A	XP_011530439.1:p.Ala433Thr
XM_011532138.1:c.1297G>A	XP_011530440.1:p.Ala433Thr
XM_011532139.1:c.1297G>A	XP_011530441.1:p.Ala433Thr
XM_011532140.1:c.1297G>A	XP_011530442.1:p.Ala433Thr
XM_011532141.1:c.1159G>A	XP_011530443.1:p.Ala387Thr
XM_011532142.1:c.1138G>A	XP_011530444.1:p.Ala380Thr
XM_005263146.4:c.742G>A	XP_005263203.1:p.Ala248Thr
XM_011532133.2:c.1585G>A	XP_011530435.1:p.Ala529Thr
XM_011532135.2:c.1444G>A	XP_011530437.1:p.Ala482Thr
XM_011532140.2:c.1297G>A	XP_011530442.1:p.Ala433Thr
XM_011532141.3:c.1159G>A	XP_011530443.1:p.Ala387Thr
XM_017008468.1:c.1294G>A	XP_016863957.1:p.Ala432Thr
XM_017008469.1:c.1381G>A	XP_016863958.1:p.Ala461Thr
XM_017008470.1:c.1297G>A	XP_016863959.1:p.Ala433Thr
NM_001099403.2:c.742G>A MANE Select	NP_001092873.1:p.Ala248Thr
NM_020226.4:c.742G>A	NP_064611.3:p.Ala248Thr