Canonical Allele Identifier: CA1471291776

Gene: PRDM8

Linked Data

• ClinVar Variation Id: 1670346
• ClinVar RCV Id: RCV002203637
• dbSNP Id: rs777390514

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80201895G>T , CM000666.2:g.80201895G>T	GRCh38
NC_000004.11:g.81123049G>T , CM000666.1:g.81123049G>T	GRCh37
NC_000004.10:g.81342073G>T	NCBI36
NG_046725.1:g.21626G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.452-19G>T MANE Select	ENSP00000406998.2:n.452-19G>T
ENST00000339711.8:c.452-19G>T	ENSP00000339764.4:n.452-19G>T
ENST00000415738.2:c.452-19G>T	ENSP00000406998.2:n.452-19G>T
ENST00000504452.5:c.452-19G>T	ENSP00000423985.1:n.452-19G>T
ENST00000515013.5:c.452-19G>T	ENSP00000425149.1:n.452-19G>T
NM_001099403.1:c.452-19G>T	NP_001092873.1:n.452-19G>T
NM_020226.3:c.452-19G>T	NP_064611.3:n.452-19G>T
XM_005263144.2:c.452-16G>T	XP_005263201.1:n.452-16G>T
XM_005263145.2:c.452-16G>T	XP_005263202.1:n.452-16G>T
XM_005263146.3:c.452-19G>T	XP_005263203.1:n.452-19G>T
XM_011532133.1:c.1292-16G>T	XP_011530435.1:n.1292-16G>T
XM_011532134.1:c.1292-19G>T	XP_011530436.1:n.1292-19G>T
XM_011532135.1:c.1151-16G>T	XP_011530437.1:n.1151-16G>T
XM_011532136.1:c.1004-16G>T	XP_011530438.1:n.1004-16G>T
XM_011532137.1:c.1004-16G>T	XP_011530439.1:n.1004-16G>T
XM_011532138.1:c.1004-16G>T	XP_011530440.1:n.1004-16G>T
XM_011532139.1:c.1004-16G>T	XP_011530441.1:n.1004-16G>T
XM_011532140.1:c.1004-16G>T	XP_011530442.1:n.1004-16G>T
XM_011532141.1:c.866-16G>T	XP_011530443.1:n.866-16G>T
XM_011532142.1:c.845-16G>T	XP_011530444.1:n.845-16G>T
XM_005263146.4:c.452-19G>T	XP_005263203.1:n.452-19G>T
XM_011532133.2:c.1292-16G>T	XP_011530435.1:n.1292-16G>T
XM_011532135.2:c.1151-16G>T	XP_011530437.1:n.1151-16G>T
XM_011532140.2:c.1004-16G>T	XP_011530442.1:n.1004-16G>T
XM_011532141.3:c.866-16G>T	XP_011530443.1:n.866-16G>T
XM_017008468.1:c.1004-19G>T	XP_016863957.1:n.1004-19G>T
XM_017008469.1:c.1088-16G>T	XP_016863958.1:n.1088-16G>T
XM_017008470.1:c.1004-16G>T	XP_016863959.1:n.1004-16G>T
NM_001099403.2:c.452-19G>T MANE Select	NP_001092873.1:n.452-19G>T
NM_020226.4:c.452-19G>T	NP_064611.3:n.452-19G>T