Canonical Allele Identifier: CA440226725

Gene: PRDM8

Linked Data

• gnomAD v4: 4-80202377-C-T
• COSMIC: COSM1310294
• MyVariant Identifiers: chr4:g.81123531C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202377C>T , CM000666.2:g.80202377C>T	GRCh38
NC_000004.11:g.81123531C>T , CM000666.1:g.81123531C>T	GRCh37
NC_000004.10:g.81342555C>T	NCBI36
NG_046725.1:g.22108C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.915C>T MANE Select	ENSP00000406998.2:p.Ile305=
ENST00000339711.8:c.915C>T	ENSP00000339764.4:p.Ile305=
ENST00000415738.2:c.915C>T	ENSP00000406998.2:p.Ile305=
ENST00000504452.5:c.915C>T	ENSP00000423985.1:p.Ile305=
ENST00000515013.5:c.915C>T	ENSP00000425149.1:p.Ile305=
NM_001099403.1:c.915C>T	NP_001092873.1:p.Ile305=
NM_020226.3:c.915C>T	NP_064611.3:p.Ile305=
XM_005263144.2:c.918C>T	XP_005263201.1:p.Ile306=
XM_005263145.2:c.918C>T	XP_005263202.1:p.Ile306=
XM_005263146.3:c.915C>T	XP_005263203.1:p.Ile305=
XM_011532133.1:c.1758C>T	XP_011530435.1:p.Ile586=
XM_011532134.1:c.1755C>T	XP_011530436.1:p.Ile585=
XM_011532135.1:c.1617C>T	XP_011530437.1:p.Ile539=
XM_011532136.1:c.1470C>T	XP_011530438.1:p.Ile490=
XM_011532137.1:c.1470C>T	XP_011530439.1:p.Ile490=
XM_011532138.1:c.1470C>T	XP_011530440.1:p.Ile490=
XM_011532139.1:c.1470C>T	XP_011530441.1:p.Ile490=
XM_011532140.1:c.1470C>T	XP_011530442.1:p.Ile490=
XM_011532141.1:c.1332C>T	XP_011530443.1:p.Ile444=
XM_011532142.1:c.1311C>T	XP_011530444.1:p.Ile437=
XM_005263146.4:c.915C>T	XP_005263203.1:p.Ile305=
XM_011532133.2:c.1758C>T	XP_011530435.1:p.Ile586=
XM_011532135.2:c.1617C>T	XP_011530437.1:p.Ile539=
XM_011532140.2:c.1470C>T	XP_011530442.1:p.Ile490=
XM_011532141.3:c.1332C>T	XP_011530443.1:p.Ile444=
XM_017008468.1:c.1467C>T	XP_016863957.1:p.Ile489=
XM_017008469.1:c.1554C>T	XP_016863958.1:p.Ile518=
XM_017008470.1:c.1470C>T	XP_016863959.1:p.Ile490=
NM_001099403.2:c.915C>T MANE Select	NP_001092873.1:p.Ile305=
NM_020226.4:c.915C>T	NP_064611.3:p.Ile305=