Canonical Allele Identifier: CA357395583

Gene: PRDM8

Linked Data

• gnomAD v4: 4-80202355-C-T
• MyVariant Identifiers: chr4:g.81123509C>T (hg19) ; chr4:g.80202355C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202355C>T , CM000666.2:g.80202355C>T	GRCh38
NC_000004.11:g.81123509C>T , CM000666.1:g.81123509C>T	GRCh37
NC_000004.10:g.81342533C>T	NCBI36
NG_046725.1:g.22086C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.893C>T MANE Select	ENSP00000406998.2:p.Ala298Val
ENST00000339711.8:c.893C>T	ENSP00000339764.4:p.Ala298Val
ENST00000415738.2:c.893C>T	ENSP00000406998.2:p.Ala298Val
ENST00000504452.5:c.893C>T	ENSP00000423985.1:p.Ala298Val
ENST00000515013.5:c.893C>T	ENSP00000425149.1:p.Ala298Val
NM_001099403.1:c.893C>T	NP_001092873.1:p.Ala298Val
NM_020226.3:c.893C>T	NP_064611.3:p.Ala298Val
XM_005263144.2:c.896C>T	XP_005263201.1:p.Ala299Val
XM_005263145.2:c.896C>T	XP_005263202.1:p.Ala299Val
XM_005263146.3:c.893C>T	XP_005263203.1:p.Ala298Val
XM_011532133.1:c.1736C>T	XP_011530435.1:p.Ala579Val
XM_011532134.1:c.1733C>T	XP_011530436.1:p.Ala578Val
XM_011532135.1:c.1595C>T	XP_011530437.1:p.Ala532Val
XM_011532136.1:c.1448C>T	XP_011530438.1:p.Ala483Val
XM_011532137.1:c.1448C>T	XP_011530439.1:p.Ala483Val
XM_011532138.1:c.1448C>T	XP_011530440.1:p.Ala483Val
XM_011532139.1:c.1448C>T	XP_011530441.1:p.Ala483Val
XM_011532140.1:c.1448C>T	XP_011530442.1:p.Ala483Val
XM_011532141.1:c.1310C>T	XP_011530443.1:p.Ala437Val
XM_011532142.1:c.1289C>T	XP_011530444.1:p.Ala430Val
XM_005263146.4:c.893C>T	XP_005263203.1:p.Ala298Val
XM_011532133.2:c.1736C>T	XP_011530435.1:p.Ala579Val
XM_011532135.2:c.1595C>T	XP_011530437.1:p.Ala532Val
XM_011532140.2:c.1448C>T	XP_011530442.1:p.Ala483Val
XM_011532141.3:c.1310C>T	XP_011530443.1:p.Ala437Val
XM_017008468.1:c.1445C>T	XP_016863957.1:p.Ala482Val
XM_017008469.1:c.1532C>T	XP_016863958.1:p.Ala511Val
XM_017008470.1:c.1448C>T	XP_016863959.1:p.Ala483Val
NM_001099403.2:c.893C>T MANE Select	NP_001092873.1:p.Ala298Val
NM_020226.4:c.893C>T	NP_064611.3:p.Ala298Val