Canonical Allele Identifier: CA357395225

Gene: PRDM8

Linked Data

• MyVariant Identifiers: chr4:g.81123404A>C (hg19) ; chr4:g.80202250A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202250A>C , CM000666.2:g.80202250A>C	GRCh38
NC_000004.11:g.81123404A>C , CM000666.1:g.81123404A>C	GRCh37
NC_000004.10:g.81342428A>C	NCBI36
NG_046725.1:g.21981A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.788A>C MANE Select	ENSP00000406998.2:p.Asn263Thr
ENST00000339711.8:c.788A>C	ENSP00000339764.4:p.Asn263Thr
ENST00000415738.2:c.788A>C	ENSP00000406998.2:p.Asn263Thr
ENST00000504452.5:c.788A>C	ENSP00000423985.1:p.Asn263Thr
ENST00000515013.5:c.788A>C	ENSP00000425149.1:p.Asn263Thr
NM_001099403.1:c.788A>C	NP_001092873.1:p.Asn263Thr
NM_020226.3:c.788A>C	NP_064611.3:p.Asn263Thr
XM_005263144.2:c.791A>C	XP_005263201.1:p.Asn264Thr
XM_005263145.2:c.791A>C	XP_005263202.1:p.Asn264Thr
XM_005263146.3:c.788A>C	XP_005263203.1:p.Asn263Thr
XM_011532133.1:c.1631A>C	XP_011530435.1:p.Asn544Thr
XM_011532134.1:c.1628A>C	XP_011530436.1:p.Asn543Thr
XM_011532135.1:c.1490A>C	XP_011530437.1:p.Asn497Thr
XM_011532136.1:c.1343A>C	XP_011530438.1:p.Asn448Thr
XM_011532137.1:c.1343A>C	XP_011530439.1:p.Asn448Thr
XM_011532138.1:c.1343A>C	XP_011530440.1:p.Asn448Thr
XM_011532139.1:c.1343A>C	XP_011530441.1:p.Asn448Thr
XM_011532140.1:c.1343A>C	XP_011530442.1:p.Asn448Thr
XM_011532141.1:c.1205A>C	XP_011530443.1:p.Asn402Thr
XM_011532142.1:c.1184A>C	XP_011530444.1:p.Asn395Thr
XM_005263146.4:c.788A>C	XP_005263203.1:p.Asn263Thr
XM_011532133.2:c.1631A>C	XP_011530435.1:p.Asn544Thr
XM_011532135.2:c.1490A>C	XP_011530437.1:p.Asn497Thr
XM_011532140.2:c.1343A>C	XP_011530442.1:p.Asn448Thr
XM_011532141.3:c.1205A>C	XP_011530443.1:p.Asn402Thr
XM_017008468.1:c.1340A>C	XP_016863957.1:p.Asn447Thr
XM_017008469.1:c.1427A>C	XP_016863958.1:p.Asn476Thr
XM_017008470.1:c.1343A>C	XP_016863959.1:p.Asn448Thr
NM_001099403.2:c.788A>C MANE Select	NP_001092873.1:p.Asn263Thr
NM_020226.4:c.788A>C	NP_064611.3:p.Asn263Thr