Canonical Allele Identifier: CA440227443
Gene: PRDM8 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.81123738A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80202584A>G , CM000666.2:g.80202584A>G GRCh38
NC_000004.11:g.81123738A>G , CM000666.1:g.81123738A>G GRCh37
NC_000004.10:g.81342762A>G NCBI36
NG_046725.1:g.22315A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000415738.3:c.1122A>G MANE Select ENSP00000406998.2:p.Pro374=
ENST00000339711.8:c.1122A>G ENSP00000339764.4:p.Pro374=
ENST00000415738.2:c.1122A>G ENSP00000406998.2:p.Pro374=
ENST00000504452.5:c.1122A>G ENSP00000423985.1:p.Pro374=
ENST00000515013.5:c.1122A>G ENSP00000425149.1:p.Pro374=
NM_001099403.1:c.1122A>G NP_001092873.1:p.Pro374=
NM_020226.3:c.1122A>G NP_064611.3:p.Pro374=
XM_005263144.2:c.1125A>G XP_005263201.1:p.Pro375=
XM_005263145.2:c.1125A>G XP_005263202.1:p.Pro375=
XM_005263146.3:c.1122A>G XP_005263203.1:p.Pro374=
XM_011532133.1:c.1965A>G XP_011530435.1:p.Pro655=
XM_011532134.1:c.1962A>G XP_011530436.1:p.Pro654=
XM_011532135.1:c.1824A>G XP_011530437.1:p.Pro608=
XM_011532136.1:c.1677A>G XP_011530438.1:p.Pro559=
XM_011532137.1:c.1677A>G XP_011530439.1:p.Pro559=
XM_011532138.1:c.1677A>G XP_011530440.1:p.Pro559=
XM_011532139.1:c.1677A>G XP_011530441.1:p.Pro559=
XM_011532140.1:c.1677A>G XP_011530442.1:p.Pro559=
XM_011532141.1:c.1539A>G XP_011530443.1:p.Pro513=
XM_011532142.1:c.1518A>G XP_011530444.1:p.Pro506=
XM_005263146.4:c.1122A>G XP_005263203.1:p.Pro374=
XM_011532133.2:c.1965A>G XP_011530435.1:p.Pro655=
XM_011532135.2:c.1824A>G XP_011530437.1:p.Pro608=
XM_011532140.2:c.1677A>G XP_011530442.1:p.Pro559=
XM_011532141.3:c.1539A>G XP_011530443.1:p.Pro513=
XM_017008468.1:c.1674A>G XP_016863957.1:p.Pro558=
XM_017008469.1:c.1761A>G XP_016863958.1:p.Pro587=
XM_017008470.1:c.1677A>G XP_016863959.1:p.Pro559=
NM_001099403.2:c.1122A>G MANE Select NP_001092873.1:p.Pro374=
NM_020226.4:c.1122A>G NP_064611.3:p.Pro374=