Canonical Allele Identifier: CA2428428157
Gene: PQBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48903044G= , CM000685.2:g.48903044G= GRCh38
NC_000023.10:g.48760321G= , CM000685.1:g.48760321G= GRCh37
NC_000023.9:g.48645265G= NCBI36
NG_015967.1:g.10127G=
NG_015968.2:g.106C=
NG_034300.1:g.13915C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000218224.9:c.758G= ENSP00000218224.4:p.Arg253=
ENST00000376563.6:c.758G= ENSP00000365747.1:p.Arg253=
ENST00000396763.6:c.758G= ENSP00000379985.1:p.Arg253=
ENST00000443648.6:c.758G= ENSP00000414861.2:p.Arg253=
ENST00000456306.2:c.149G= ENSP00000393013.2:p.Arg50=
ENST00000472742.6:c.*175G= ENSP00000509191.1:n.*175G=
ENST00000474671.6:n.1913G=
ENST00000477997.6:n.1707G=
ENST00000486150.6:n.2013G=
ENST00000692023.1:c.*1179G= ENSP00000509927.1:n.*1179G=
ENST00000447146.7:c.758G= MANE Select ENSP00000391759.2:p.Arg253=
ENST00000651767.1:c.758G= ENSP00000498362.1:p.Arg253=
ENST00000218224.8:c.758G= ENSP00000218224.4:p.Arg253=
ENST00000247140.8:c.473G= ENSP00000247140.4:p.Arg158=
ENST00000376563.5:c.758G= ENSP00000365747.1:p.Arg253=
ENST00000376566.8:c.473G= ENSP00000365750.4:p.Arg158=
ENST00000396763.5:c.758G= ENSP00000379985.1:p.Arg253=
ENST00000447146.6:c.758G= ENSP00000391759.2:p.Arg253=
ENST00000456306.1:c.439G=
ENST00000463529.4:n.1104G=
ENST00000465859.2:n.772G=
ENST00000470059.5:n.972G=
ENST00000470062.5:n.730G=
ENST00000473764.5:n.1330G=
ENST00000474671.5:n.818G=
ENST00000477997.5:n.839G=
NM_001032381.1:c.758G= NP_001027553.1:p.Arg253=
NM_001032382.1:c.758G= NP_001027554.1:p.Arg253=
NM_001032383.1:c.758G= NP_001027555.1:p.Arg253=
NM_001032384.1:c.758G= NP_001027556.1:p.Arg253=
NM_001167989.1:c.755G= NP_001161461.1:p.Arg252=
NM_001167990.1:c.734G= NP_001161462.1:p.Arg245=
NM_001167992.1:c.458G= NP_001161464.1:p.Arg153=
NM_005710.2:c.758G= NP_005701.1:p.Arg253=
NM_144495.2:c.473G= NP_652766.1:p.Arg158=
XM_005272571.3:c.755G= XP_005272628.1:p.Arg252=
XM_005272572.3:c.473G= XP_005272629.1:p.Arg158=
XM_011543884.1:c.758G= XP_011542186.1:p.Arg253=
XM_005272572.4:c.473G= XP_005272629.1:p.Arg158=
XM_011543884.2:c.758G= XP_011542186.1:p.Arg253=
XM_017029207.1:c.755G= XP_016884696.1:p.Arg252=
NM_001032381.2:c.758G= NP_001027553.1:p.Arg253=
NM_001032382.2:c.758G= MANE Select NP_001027554.1:p.Arg253=
NM_001032383.2:c.758G= NP_001027555.1:p.Arg253=
NM_001167989.2:c.755G= NP_001161461.1:p.Arg252=
NM_001167990.2:c.734G= NP_001161462.1:p.Arg245=
NM_144495.3:c.473G= NP_652766.1:p.Arg158=