Canonical Allele Identifier: CA439983317
Gene: PRDM8 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80200161C>T , CM000666.2:g.80200161C>T GRCh38
NC_000004.11:g.81121315C>T , CM000666.1:g.81121315C>T GRCh37
NC_000004.10:g.81340339C>T NCBI36
NG_046725.1:g.19892C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000415738.3:c.81C>T MANE Select ENSP00000406998.2:p.Thr27=
ENST00000339711.8:c.81C>T ENSP00000339764.4:p.Thr27=
ENST00000415738.2:c.81C>T ENSP00000406998.2:p.Thr27=
ENST00000504452.5:c.81C>T ENSP00000423985.1:p.Thr27=
ENST00000515013.5:c.81C>T ENSP00000425149.1:p.Thr27=
NM_001099403.1:c.81C>T NP_001092873.1:p.Thr27=
NM_020226.3:c.81C>T NP_064611.3:p.Thr27=
XM_005263144.2:c.81C>T XP_005263201.1:p.Thr27=
XM_005263145.2:c.81C>T XP_005263202.1:p.Thr27=
XM_005263146.3:c.81C>T XP_005263203.1:p.Thr27=
XM_011532133.1:c.921C>T XP_011530435.1:p.Thr307=
XM_011532134.1:c.921C>T XP_011530436.1:p.Thr307=
XM_011532135.1:c.780C>T XP_011530437.1:p.Thr260=
XM_011532136.1:c.633C>T XP_011530438.1:p.Thr211=
XM_011532137.1:c.633C>T XP_011530439.1:p.Thr211=
XM_011532138.1:c.633C>T XP_011530440.1:p.Thr211=
XM_011532139.1:c.633C>T XP_011530441.1:p.Thr211=
XM_011532140.1:c.633C>T XP_011530442.1:p.Thr211=
XM_011532141.1:c.495C>T XP_011530443.1:p.Thr165=
XM_011532142.1:c.474C>T XP_011530444.1:p.Thr158=
XM_005263146.4:c.81C>T XP_005263203.1:p.Thr27=
XM_011532133.2:c.921C>T XP_011530435.1:p.Thr307=
XM_011532135.2:c.780C>T XP_011530437.1:p.Thr260=
XM_011532140.2:c.633C>T XP_011530442.1:p.Thr211=
XM_011532141.3:c.495C>T XP_011530443.1:p.Thr165=
XM_017008468.1:c.633C>T XP_016863957.1:p.Thr211=
XM_017008469.1:c.717C>T XP_016863958.1:p.Thr239=
XM_017008470.1:c.633C>T XP_016863959.1:p.Thr211=
NM_001099403.2:c.81C>T MANE Select NP_001092873.1:p.Thr27=
NM_020226.4:c.81C>T NP_064611.3:p.Thr27=