Canonical Allele Identifier: CA357395275

Gene: PRDM8

Linked Data

• MyVariant Identifiers: chr4:g.81123427T>A (hg19) ; chr4:g.80202273T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202273T>A , CM000666.2:g.80202273T>A	GRCh38
NC_000004.11:g.81123427T>A , CM000666.1:g.81123427T>A	GRCh37
NC_000004.10:g.81342451T>A	NCBI36
NG_046725.1:g.22004T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.811T>A MANE Select	ENSP00000406998.2:p.Ser271Thr
ENST00000339711.8:c.811T>A	ENSP00000339764.4:p.Ser271Thr
ENST00000415738.2:c.811T>A	ENSP00000406998.2:p.Ser271Thr
ENST00000504452.5:c.811T>A	ENSP00000423985.1:p.Ser271Thr
ENST00000515013.5:c.811T>A	ENSP00000425149.1:p.Ser271Thr
NM_001099403.1:c.811T>A	NP_001092873.1:p.Ser271Thr
NM_020226.3:c.811T>A	NP_064611.3:p.Ser271Thr
XM_005263144.2:c.814T>A	XP_005263201.1:p.Ser272Thr
XM_005263145.2:c.814T>A	XP_005263202.1:p.Ser272Thr
XM_005263146.3:c.811T>A	XP_005263203.1:p.Ser271Thr
XM_011532133.1:c.1654T>A	XP_011530435.1:p.Ser552Thr
XM_011532134.1:c.1651T>A	XP_011530436.1:p.Ser551Thr
XM_011532135.1:c.1513T>A	XP_011530437.1:p.Ser505Thr
XM_011532136.1:c.1366T>A	XP_011530438.1:p.Ser456Thr
XM_011532137.1:c.1366T>A	XP_011530439.1:p.Ser456Thr
XM_011532138.1:c.1366T>A	XP_011530440.1:p.Ser456Thr
XM_011532139.1:c.1366T>A	XP_011530441.1:p.Ser456Thr
XM_011532140.1:c.1366T>A	XP_011530442.1:p.Ser456Thr
XM_011532141.1:c.1228T>A	XP_011530443.1:p.Ser410Thr
XM_011532142.1:c.1207T>A	XP_011530444.1:p.Ser403Thr
XM_005263146.4:c.811T>A	XP_005263203.1:p.Ser271Thr
XM_011532133.2:c.1654T>A	XP_011530435.1:p.Ser552Thr
XM_011532135.2:c.1513T>A	XP_011530437.1:p.Ser505Thr
XM_011532140.2:c.1366T>A	XP_011530442.1:p.Ser456Thr
XM_011532141.3:c.1228T>A	XP_011530443.1:p.Ser410Thr
XM_017008468.1:c.1363T>A	XP_016863957.1:p.Ser455Thr
XM_017008469.1:c.1450T>A	XP_016863958.1:p.Ser484Thr
XM_017008470.1:c.1366T>A	XP_016863959.1:p.Ser456Thr
NM_001099403.2:c.811T>A MANE Select	NP_001092873.1:p.Ser271Thr
NM_020226.4:c.811T>A	NP_064611.3:p.Ser271Thr