Canonical Allele Identifier: CA357398044

Gene: PRDM8

Linked Data

• gnomAD v4: 4-80202529-G-C
• MyVariant Identifiers: chr4:g.81123683G>C (hg19) ; chr4:g.80202529G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202529G>C , CM000666.2:g.80202529G>C	GRCh38
NC_000004.11:g.81123683G>C , CM000666.1:g.81123683G>C	GRCh37
NC_000004.10:g.81342707G>C	NCBI36
NG_046725.1:g.22260G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.1067G>C MANE Select	ENSP00000406998.2:p.Arg356Pro
ENST00000339711.8:c.1067G>C	ENSP00000339764.4:p.Arg356Pro
ENST00000415738.2:c.1067G>C	ENSP00000406998.2:p.Arg356Pro
ENST00000504452.5:c.1067G>C	ENSP00000423985.1:p.Arg356Pro
ENST00000515013.5:c.1067G>C	ENSP00000425149.1:p.Arg356Pro
NM_001099403.1:c.1067G>C	NP_001092873.1:p.Arg356Pro
NM_020226.3:c.1067G>C	NP_064611.3:p.Arg356Pro
XM_005263144.2:c.1070G>C	XP_005263201.1:p.Arg357Pro
XM_005263145.2:c.1070G>C	XP_005263202.1:p.Arg357Pro
XM_005263146.3:c.1067G>C	XP_005263203.1:p.Arg356Pro
XM_011532133.1:c.1910G>C	XP_011530435.1:p.Arg637Pro
XM_011532134.1:c.1907G>C	XP_011530436.1:p.Arg636Pro
XM_011532135.1:c.1769G>C	XP_011530437.1:p.Arg590Pro
XM_011532136.1:c.1622G>C	XP_011530438.1:p.Arg541Pro
XM_011532137.1:c.1622G>C	XP_011530439.1:p.Arg541Pro
XM_011532138.1:c.1622G>C	XP_011530440.1:p.Arg541Pro
XM_011532139.1:c.1622G>C	XP_011530441.1:p.Arg541Pro
XM_011532140.1:c.1622G>C	XP_011530442.1:p.Arg541Pro
XM_011532141.1:c.1484G>C	XP_011530443.1:p.Arg495Pro
XM_011532142.1:c.1463G>C	XP_011530444.1:p.Arg488Pro
XM_005263146.4:c.1067G>C	XP_005263203.1:p.Arg356Pro
XM_011532133.2:c.1910G>C	XP_011530435.1:p.Arg637Pro
XM_011532135.2:c.1769G>C	XP_011530437.1:p.Arg590Pro
XM_011532140.2:c.1622G>C	XP_011530442.1:p.Arg541Pro
XM_011532141.3:c.1484G>C	XP_011530443.1:p.Arg495Pro
XM_017008468.1:c.1619G>C	XP_016863957.1:p.Arg540Pro
XM_017008469.1:c.1706G>C	XP_016863958.1:p.Arg569Pro
XM_017008470.1:c.1622G>C	XP_016863959.1:p.Arg541Pro
NM_001099403.2:c.1067G>C MANE Select	NP_001092873.1:p.Arg356Pro
NM_020226.4:c.1067G>C	NP_064611.3:p.Arg356Pro