Canonical Allele Identifier: CA357398251

Gene: PRDM8

Linked Data

• gnomAD v4: 4-80202562-A-C
• MyVariant Identifiers: chr4:g.81123716A>C (hg19) ; chr4:g.80202562A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202562A>C , CM000666.2:g.80202562A>C	GRCh38
NC_000004.11:g.81123716A>C , CM000666.1:g.81123716A>C	GRCh37
NC_000004.10:g.81342740A>C	NCBI36
NG_046725.1:g.22293A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.1100A>C MANE Select	ENSP00000406998.2:p.Asn367Thr
ENST00000339711.8:c.1100A>C	ENSP00000339764.4:p.Asn367Thr
ENST00000415738.2:c.1100A>C	ENSP00000406998.2:p.Asn367Thr
ENST00000504452.5:c.1100A>C	ENSP00000423985.1:p.Asn367Thr
ENST00000515013.5:c.1100A>C	ENSP00000425149.1:p.Asn367Thr
NM_001099403.1:c.1100A>C	NP_001092873.1:p.Asn367Thr
NM_020226.3:c.1100A>C	NP_064611.3:p.Asn367Thr
XM_005263144.2:c.1103A>C	XP_005263201.1:p.Asn368Thr
XM_005263145.2:c.1103A>C	XP_005263202.1:p.Asn368Thr
XM_005263146.3:c.1100A>C	XP_005263203.1:p.Asn367Thr
XM_011532133.1:c.1943A>C	XP_011530435.1:p.Asn648Thr
XM_011532134.1:c.1940A>C	XP_011530436.1:p.Asn647Thr
XM_011532135.1:c.1802A>C	XP_011530437.1:p.Asn601Thr
XM_011532136.1:c.1655A>C	XP_011530438.1:p.Asn552Thr
XM_011532137.1:c.1655A>C	XP_011530439.1:p.Asn552Thr
XM_011532138.1:c.1655A>C	XP_011530440.1:p.Asn552Thr
XM_011532139.1:c.1655A>C	XP_011530441.1:p.Asn552Thr
XM_011532140.1:c.1655A>C	XP_011530442.1:p.Asn552Thr
XM_011532141.1:c.1517A>C	XP_011530443.1:p.Asn506Thr
XM_011532142.1:c.1496A>C	XP_011530444.1:p.Asn499Thr
XM_005263146.4:c.1100A>C	XP_005263203.1:p.Asn367Thr
XM_011532133.2:c.1943A>C	XP_011530435.1:p.Asn648Thr
XM_011532135.2:c.1802A>C	XP_011530437.1:p.Asn601Thr
XM_011532140.2:c.1655A>C	XP_011530442.1:p.Asn552Thr
XM_011532141.3:c.1517A>C	XP_011530443.1:p.Asn506Thr
XM_017008468.1:c.1652A>C	XP_016863957.1:p.Asn551Thr
XM_017008469.1:c.1739A>C	XP_016863958.1:p.Asn580Thr
XM_017008470.1:c.1655A>C	XP_016863959.1:p.Asn552Thr
NM_001099403.2:c.1100A>C MANE Select	NP_001092873.1:p.Asn367Thr
NM_020226.4:c.1100A>C	NP_064611.3:p.Asn367Thr