Canonical Allele Identifier: CA357398223

Gene: PRDM8

Linked Data

• MyVariant Identifiers: chr4:g.81123713A>C (hg19) ; chr4:g.80202559A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202559A>C , CM000666.2:g.80202559A>C	GRCh38
NC_000004.11:g.81123713A>C , CM000666.1:g.81123713A>C	GRCh37
NC_000004.10:g.81342737A>C	NCBI36
NG_046725.1:g.22290A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.1097A>C MANE Select	ENSP00000406998.2:p.Glu366Ala
ENST00000339711.8:c.1097A>C	ENSP00000339764.4:p.Glu366Ala
ENST00000415738.2:c.1097A>C	ENSP00000406998.2:p.Glu366Ala
ENST00000504452.5:c.1097A>C	ENSP00000423985.1:p.Glu366Ala
ENST00000515013.5:c.1097A>C	ENSP00000425149.1:p.Glu366Ala
NM_001099403.1:c.1097A>C	NP_001092873.1:p.Glu366Ala
NM_020226.3:c.1097A>C	NP_064611.3:p.Glu366Ala
XM_005263144.2:c.1100A>C	XP_005263201.1:p.Glu367Ala
XM_005263145.2:c.1100A>C	XP_005263202.1:p.Glu367Ala
XM_005263146.3:c.1097A>C	XP_005263203.1:p.Glu366Ala
XM_011532133.1:c.1940A>C	XP_011530435.1:p.Glu647Ala
XM_011532134.1:c.1937A>C	XP_011530436.1:p.Glu646Ala
XM_011532135.1:c.1799A>C	XP_011530437.1:p.Glu600Ala
XM_011532136.1:c.1652A>C	XP_011530438.1:p.Glu551Ala
XM_011532137.1:c.1652A>C	XP_011530439.1:p.Glu551Ala
XM_011532138.1:c.1652A>C	XP_011530440.1:p.Glu551Ala
XM_011532139.1:c.1652A>C	XP_011530441.1:p.Glu551Ala
XM_011532140.1:c.1652A>C	XP_011530442.1:p.Glu551Ala
XM_011532141.1:c.1514A>C	XP_011530443.1:p.Glu505Ala
XM_011532142.1:c.1493A>C	XP_011530444.1:p.Glu498Ala
XM_005263146.4:c.1097A>C	XP_005263203.1:p.Glu366Ala
XM_011532133.2:c.1940A>C	XP_011530435.1:p.Glu647Ala
XM_011532135.2:c.1799A>C	XP_011530437.1:p.Glu600Ala
XM_011532140.2:c.1652A>C	XP_011530442.1:p.Glu551Ala
XM_011532141.3:c.1514A>C	XP_011530443.1:p.Glu505Ala
XM_017008468.1:c.1649A>C	XP_016863957.1:p.Glu550Ala
XM_017008469.1:c.1736A>C	XP_016863958.1:p.Glu579Ala
XM_017008470.1:c.1652A>C	XP_016863959.1:p.Glu551Ala
NM_001099403.2:c.1097A>C MANE Select	NP_001092873.1:p.Glu366Ala
NM_020226.4:c.1097A>C	NP_064611.3:p.Glu366Ala