Canonical Allele Identifier: CA357395215

Gene: PRDM8

Linked Data

• MyVariant Identifiers: chr4:g.81123400C>G (hg19) ; chr4:g.80202246C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202246C>G , CM000666.2:g.80202246C>G	GRCh38
NC_000004.11:g.81123400C>G , CM000666.1:g.81123400C>G	GRCh37
NC_000004.10:g.81342424C>G	NCBI36
NG_046725.1:g.21977C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000415738.3:c.784C>G MANE Select	ENSP00000406998.2:p.His262Asp
ENST00000339711.8:c.784C>G	ENSP00000339764.4:p.His262Asp
ENST00000415738.2:c.784C>G	ENSP00000406998.2:p.His262Asp
ENST00000504452.5:c.784C>G	ENSP00000423985.1:p.His262Asp
ENST00000515013.5:c.784C>G	ENSP00000425149.1:p.His262Asp
NM_001099403.1:c.784C>G	NP_001092873.1:p.His262Asp
NM_020226.3:c.784C>G	NP_064611.3:p.His262Asp
XM_005263144.2:c.787C>G	XP_005263201.1:p.His263Asp
XM_005263145.2:c.787C>G	XP_005263202.1:p.His263Asp
XM_005263146.3:c.784C>G	XP_005263203.1:p.His262Asp
XM_011532133.1:c.1627C>G	XP_011530435.1:p.His543Asp
XM_011532134.1:c.1624C>G	XP_011530436.1:p.His542Asp
XM_011532135.1:c.1486C>G	XP_011530437.1:p.His496Asp
XM_011532136.1:c.1339C>G	XP_011530438.1:p.His447Asp
XM_011532137.1:c.1339C>G	XP_011530439.1:p.His447Asp
XM_011532138.1:c.1339C>G	XP_011530440.1:p.His447Asp
XM_011532139.1:c.1339C>G	XP_011530441.1:p.His447Asp
XM_011532140.1:c.1339C>G	XP_011530442.1:p.His447Asp
XM_011532141.1:c.1201C>G	XP_011530443.1:p.His401Asp
XM_011532142.1:c.1180C>G	XP_011530444.1:p.His394Asp
XM_005263146.4:c.784C>G	XP_005263203.1:p.His262Asp
XM_011532133.2:c.1627C>G	XP_011530435.1:p.His543Asp
XM_011532135.2:c.1486C>G	XP_011530437.1:p.His496Asp
XM_011532140.2:c.1339C>G	XP_011530442.1:p.His447Asp
XM_011532141.3:c.1201C>G	XP_011530443.1:p.His401Asp
XM_017008468.1:c.1336C>G	XP_016863957.1:p.His446Asp
XM_017008469.1:c.1423C>G	XP_016863958.1:p.His475Asp
XM_017008470.1:c.1339C>G	XP_016863959.1:p.His447Asp
NM_001099403.2:c.784C>G MANE Select	NP_001092873.1:p.His262Asp
NM_020226.4:c.784C>G	NP_064611.3:p.His262Asp