Canonical Allele Identifier: CA2573138353

Gene: PRDM8

Linked Data

• ClinVar Variation Id: 1672842
• ClinVar RCV Id: RCV002210758
• dbSNP Id: rs2109877266

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80201541G>A , CM000666.2:g.80201541G>A	GRCh38
NC_000004.11:g.81122695G>A , CM000666.1:g.81122695G>A	GRCh37
NC_000004.10:g.81341719G>A	NCBI36
NG_046725.1:g.21272G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.451+20G>A MANE Select	ENSP00000406998.2:n.451+20G>A
ENST00000339711.8:c.451+20G>A	ENSP00000339764.4:n.451+20G>A
ENST00000415738.2:c.451+20G>A	ENSP00000406998.2:n.451+20G>A
ENST00000504452.5:c.451+20G>A	ENSP00000423985.1:n.451+20G>A
ENST00000515013.5:c.451+20G>A	ENSP00000425149.1:n.451+20G>A
NM_001099403.1:c.451+20G>A	NP_001092873.1:n.451+20G>A
NM_020226.3:c.451+20G>A	NP_064611.3:n.451+20G>A
XM_005263144.2:c.451+20G>A	XP_005263201.1:n.451+20G>A
XM_005263145.2:c.451+20G>A	XP_005263202.1:n.451+20G>A
XM_005263146.3:c.451+20G>A	XP_005263203.1:n.451+20G>A
XM_011532133.1:c.1291+20G>A	XP_011530435.1:n.1291+20G>A
XM_011532134.1:c.1291+20G>A	XP_011530436.1:n.1291+20G>A
XM_011532135.1:c.1150+20G>A	XP_011530437.1:n.1150+20G>A
XM_011532136.1:c.1003+20G>A	XP_011530438.1:n.1003+20G>A
XM_011532137.1:c.1003+20G>A	XP_011530439.1:n.1003+20G>A
XM_011532138.1:c.1003+20G>A	XP_011530440.1:n.1003+20G>A
XM_011532139.1:c.1003+20G>A	XP_011530441.1:n.1003+20G>A
XM_011532140.1:c.1003+20G>A	XP_011530442.1:n.1003+20G>A
XM_011532141.1:c.865+20G>A	XP_011530443.1:n.865+20G>A
XM_011532142.1:c.844+20G>A	XP_011530444.1:n.844+20G>A
XM_005263146.4:c.451+20G>A	XP_005263203.1:n.451+20G>A
XM_011532133.2:c.1291+20G>A	XP_011530435.1:n.1291+20G>A
XM_011532135.2:c.1150+20G>A	XP_011530437.1:n.1150+20G>A
XM_011532140.2:c.1003+20G>A	XP_011530442.1:n.1003+20G>A
XM_011532141.3:c.865+20G>A	XP_011530443.1:n.865+20G>A
XM_017008468.1:c.1003+20G>A	XP_016863957.1:n.1003+20G>A
XM_017008469.1:c.1087+20G>A	XP_016863958.1:n.1087+20G>A
XM_017008470.1:c.1003+20G>A	XP_016863959.1:n.1003+20G>A
NM_001099403.2:c.451+20G>A MANE Select	NP_001092873.1:n.451+20G>A
NM_020226.4:c.451+20G>A	NP_064611.3:n.451+20G>A