Canonical Allele Identifier: CA357396741

Gene: PRDM8

Linked Data

• gnomAD v4: 4-80202373-G-T
• MyVariant Identifiers: chr4:g.81123527G>T (hg19) ; chr4:g.80202373G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202373G>T , CM000666.2:g.80202373G>T	GRCh38
NC_000004.11:g.81123527G>T , CM000666.1:g.81123527G>T	GRCh37
NC_000004.10:g.81342551G>T	NCBI36
NG_046725.1:g.22104G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.911G>T MANE Select	ENSP00000406998.2:p.Gly304Val
ENST00000339711.8:c.911G>T	ENSP00000339764.4:p.Gly304Val
ENST00000415738.2:c.911G>T	ENSP00000406998.2:p.Gly304Val
ENST00000504452.5:c.911G>T	ENSP00000423985.1:p.Gly304Val
ENST00000515013.5:c.911G>T	ENSP00000425149.1:p.Gly304Val
NM_001099403.1:c.911G>T	NP_001092873.1:p.Gly304Val
NM_020226.3:c.911G>T	NP_064611.3:p.Gly304Val
XM_005263144.2:c.914G>T	XP_005263201.1:p.Gly305Val
XM_005263145.2:c.914G>T	XP_005263202.1:p.Gly305Val
XM_005263146.3:c.911G>T	XP_005263203.1:p.Gly304Val
XM_011532133.1:c.1754G>T	XP_011530435.1:p.Gly585Val
XM_011532134.1:c.1751G>T	XP_011530436.1:p.Gly584Val
XM_011532135.1:c.1613G>T	XP_011530437.1:p.Gly538Val
XM_011532136.1:c.1466G>T	XP_011530438.1:p.Gly489Val
XM_011532137.1:c.1466G>T	XP_011530439.1:p.Gly489Val
XM_011532138.1:c.1466G>T	XP_011530440.1:p.Gly489Val
XM_011532139.1:c.1466G>T	XP_011530441.1:p.Gly489Val
XM_011532140.1:c.1466G>T	XP_011530442.1:p.Gly489Val
XM_011532141.1:c.1328G>T	XP_011530443.1:p.Gly443Val
XM_011532142.1:c.1307G>T	XP_011530444.1:p.Gly436Val
XM_005263146.4:c.911G>T	XP_005263203.1:p.Gly304Val
XM_011532133.2:c.1754G>T	XP_011530435.1:p.Gly585Val
XM_011532135.2:c.1613G>T	XP_011530437.1:p.Gly538Val
XM_011532140.2:c.1466G>T	XP_011530442.1:p.Gly489Val
XM_011532141.3:c.1328G>T	XP_011530443.1:p.Gly443Val
XM_017008468.1:c.1463G>T	XP_016863957.1:p.Gly488Val
XM_017008469.1:c.1550G>T	XP_016863958.1:p.Gly517Val
XM_017008470.1:c.1466G>T	XP_016863959.1:p.Gly489Val
NM_001099403.2:c.911G>T MANE Select	NP_001092873.1:p.Gly304Val
NM_020226.4:c.911G>T	NP_064611.3:p.Gly304Val