Canonical Allele Identifier: CA440226861

Gene: PRDM8

Linked Data

• gnomAD v4: 4-80202248-C-T
• MyVariant Identifiers: chr4:g.81123402C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202248C>T , CM000666.2:g.80202248C>T	GRCh38
NC_000004.11:g.81123402C>T , CM000666.1:g.81123402C>T	GRCh37
NC_000004.10:g.81342426C>T	NCBI36
NG_046725.1:g.21979C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000415738.3:c.786C>T MANE Select	ENSP00000406998.2:p.His262=
ENST00000339711.8:c.786C>T	ENSP00000339764.4:p.His262=
ENST00000415738.2:c.786C>T	ENSP00000406998.2:p.His262=
ENST00000504452.5:c.786C>T	ENSP00000423985.1:p.His262=
ENST00000515013.5:c.786C>T	ENSP00000425149.1:p.His262=
NM_001099403.1:c.786C>T	NP_001092873.1:p.His262=
NM_020226.3:c.786C>T	NP_064611.3:p.His262=
XM_005263144.2:c.789C>T	XP_005263201.1:p.His263=
XM_005263145.2:c.789C>T	XP_005263202.1:p.His263=
XM_005263146.3:c.786C>T	XP_005263203.1:p.His262=
XM_011532133.1:c.1629C>T	XP_011530435.1:p.His543=
XM_011532134.1:c.1626C>T	XP_011530436.1:p.His542=
XM_011532135.1:c.1488C>T	XP_011530437.1:p.His496=
XM_011532136.1:c.1341C>T	XP_011530438.1:p.His447=
XM_011532137.1:c.1341C>T	XP_011530439.1:p.His447=
XM_011532138.1:c.1341C>T	XP_011530440.1:p.His447=
XM_011532139.1:c.1341C>T	XP_011530441.1:p.His447=
XM_011532140.1:c.1341C>T	XP_011530442.1:p.His447=
XM_011532141.1:c.1203C>T	XP_011530443.1:p.His401=
XM_011532142.1:c.1182C>T	XP_011530444.1:p.His394=
XM_005263146.4:c.786C>T	XP_005263203.1:p.His262=
XM_011532133.2:c.1629C>T	XP_011530435.1:p.His543=
XM_011532135.2:c.1488C>T	XP_011530437.1:p.His496=
XM_011532140.2:c.1341C>T	XP_011530442.1:p.His447=
XM_011532141.3:c.1203C>T	XP_011530443.1:p.His401=
XM_017008468.1:c.1338C>T	XP_016863957.1:p.His446=
XM_017008469.1:c.1425C>T	XP_016863958.1:p.His475=
XM_017008470.1:c.1341C>T	XP_016863959.1:p.His447=
NM_001099403.2:c.786C>T MANE Select	NP_001092873.1:p.His262=
NM_020226.4:c.786C>T	NP_064611.3:p.His262=