Canonical Allele Identifier: CA357398046

Gene: PRDM8

Linked Data

• MyVariant Identifiers: chr4:g.81123685G>T (hg19) ; chr4:g.80202531G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202531G>T , CM000666.2:g.80202531G>T	GRCh38
NC_000004.11:g.81123685G>T , CM000666.1:g.81123685G>T	GRCh37
NC_000004.10:g.81342709G>T	NCBI36
NG_046725.1:g.22262G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.1069G>T MANE Select	ENSP00000406998.2:p.Ala357Ser
ENST00000339711.8:c.1069G>T	ENSP00000339764.4:p.Ala357Ser
ENST00000415738.2:c.1069G>T	ENSP00000406998.2:p.Ala357Ser
ENST00000504452.5:c.1069G>T	ENSP00000423985.1:p.Ala357Ser
ENST00000515013.5:c.1069G>T	ENSP00000425149.1:p.Ala357Ser
NM_001099403.1:c.1069G>T	NP_001092873.1:p.Ala357Ser
NM_020226.3:c.1069G>T	NP_064611.3:p.Ala357Ser
XM_005263144.2:c.1072G>T	XP_005263201.1:p.Ala358Ser
XM_005263145.2:c.1072G>T	XP_005263202.1:p.Ala358Ser
XM_005263146.3:c.1069G>T	XP_005263203.1:p.Ala357Ser
XM_011532133.1:c.1912G>T	XP_011530435.1:p.Ala638Ser
XM_011532134.1:c.1909G>T	XP_011530436.1:p.Ala637Ser
XM_011532135.1:c.1771G>T	XP_011530437.1:p.Ala591Ser
XM_011532136.1:c.1624G>T	XP_011530438.1:p.Ala542Ser
XM_011532137.1:c.1624G>T	XP_011530439.1:p.Ala542Ser
XM_011532138.1:c.1624G>T	XP_011530440.1:p.Ala542Ser
XM_011532139.1:c.1624G>T	XP_011530441.1:p.Ala542Ser
XM_011532140.1:c.1624G>T	XP_011530442.1:p.Ala542Ser
XM_011532141.1:c.1486G>T	XP_011530443.1:p.Ala496Ser
XM_011532142.1:c.1465G>T	XP_011530444.1:p.Ala489Ser
XM_005263146.4:c.1069G>T	XP_005263203.1:p.Ala357Ser
XM_011532133.2:c.1912G>T	XP_011530435.1:p.Ala638Ser
XM_011532135.2:c.1771G>T	XP_011530437.1:p.Ala591Ser
XM_011532140.2:c.1624G>T	XP_011530442.1:p.Ala542Ser
XM_011532141.3:c.1486G>T	XP_011530443.1:p.Ala496Ser
XM_017008468.1:c.1621G>T	XP_016863957.1:p.Ala541Ser
XM_017008469.1:c.1708G>T	XP_016863958.1:p.Ala570Ser
XM_017008470.1:c.1624G>T	XP_016863959.1:p.Ala542Ser
NM_001099403.2:c.1069G>T MANE Select	NP_001092873.1:p.Ala357Ser
NM_020226.4:c.1069G>T	NP_064611.3:p.Ala357Ser