Canonical Allele Identifier: CA357395264

Gene: PRDM8

Linked Data

• MyVariant Identifiers: chr4:g.81123422A>T (hg19) ; chr4:g.80202268A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202268A>T , CM000666.2:g.80202268A>T	GRCh38
NC_000004.11:g.81123422A>T , CM000666.1:g.81123422A>T	GRCh37
NC_000004.10:g.81342446A>T	NCBI36
NG_046725.1:g.21999A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.806A>T MANE Select	ENSP00000406998.2:p.Glu269Val
ENST00000339711.8:c.806A>T	ENSP00000339764.4:p.Glu269Val
ENST00000415738.2:c.806A>T	ENSP00000406998.2:p.Glu269Val
ENST00000504452.5:c.806A>T	ENSP00000423985.1:p.Glu269Val
ENST00000515013.5:c.806A>T	ENSP00000425149.1:p.Glu269Val
NM_001099403.1:c.806A>T	NP_001092873.1:p.Glu269Val
NM_020226.3:c.806A>T	NP_064611.3:p.Glu269Val
XM_005263144.2:c.809A>T	XP_005263201.1:p.Glu270Val
XM_005263145.2:c.809A>T	XP_005263202.1:p.Glu270Val
XM_005263146.3:c.806A>T	XP_005263203.1:p.Glu269Val
XM_011532133.1:c.1649A>T	XP_011530435.1:p.Glu550Val
XM_011532134.1:c.1646A>T	XP_011530436.1:p.Glu549Val
XM_011532135.1:c.1508A>T	XP_011530437.1:p.Glu503Val
XM_011532136.1:c.1361A>T	XP_011530438.1:p.Glu454Val
XM_011532137.1:c.1361A>T	XP_011530439.1:p.Glu454Val
XM_011532138.1:c.1361A>T	XP_011530440.1:p.Glu454Val
XM_011532139.1:c.1361A>T	XP_011530441.1:p.Glu454Val
XM_011532140.1:c.1361A>T	XP_011530442.1:p.Glu454Val
XM_011532141.1:c.1223A>T	XP_011530443.1:p.Glu408Val
XM_011532142.1:c.1202A>T	XP_011530444.1:p.Glu401Val
XM_005263146.4:c.806A>T	XP_005263203.1:p.Glu269Val
XM_011532133.2:c.1649A>T	XP_011530435.1:p.Glu550Val
XM_011532135.2:c.1508A>T	XP_011530437.1:p.Glu503Val
XM_011532140.2:c.1361A>T	XP_011530442.1:p.Glu454Val
XM_011532141.3:c.1223A>T	XP_011530443.1:p.Glu408Val
XM_017008468.1:c.1358A>T	XP_016863957.1:p.Glu453Val
XM_017008469.1:c.1445A>T	XP_016863958.1:p.Glu482Val
XM_017008470.1:c.1361A>T	XP_016863959.1:p.Glu454Val
NM_001099403.2:c.806A>T MANE Select	NP_001092873.1:p.Glu269Val
NM_020226.4:c.806A>T	NP_064611.3:p.Glu269Val