Canonical Allele Identifier: CA2428428125
Gene: PQBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48902939C= , CM000685.2:g.48902939C= GRCh38
NC_000023.10:g.48760216C= , CM000685.1:g.48760216C= GRCh37
NC_000023.9:g.48645160C= NCBI36
NG_015967.1:g.10022C=
NG_015968.2:g.211G=
NG_034300.1:g.14020G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000218224.9:c.653C= ENSP00000218224.4:p.Ser218=
ENST00000376563.6:c.653C= ENSP00000365747.1:p.Ser218=
ENST00000396763.6:c.653C= ENSP00000379985.1:p.Ser218=
ENST00000443648.6:c.653C= ENSP00000414861.2:p.Ser218=
ENST00000456306.2:c.44C= ENSP00000393013.2:p.Ser15=
ENST00000472742.6:c.*70C= ENSP00000509191.1:n.*70C=
ENST00000474671.6:n.1808C=
ENST00000477997.6:n.1602C=
ENST00000486150.6:n.1908C=
ENST00000692023.1:c.*1074C= ENSP00000509927.1:n.*1074C=
ENST00000447146.7:c.653C= MANE Select ENSP00000391759.2:p.Ser218=
ENST00000651767.1:c.653C= ENSP00000498362.1:p.Ser218=
ENST00000218224.8:c.653C= ENSP00000218224.4:p.Ser218=
ENST00000247140.8:c.368C= ENSP00000247140.4:p.Ser123=
ENST00000376563.5:c.653C= ENSP00000365747.1:p.Ser218=
ENST00000376566.8:c.368C= ENSP00000365750.4:p.Ser123=
ENST00000396763.5:c.653C= ENSP00000379985.1:p.Ser218=
ENST00000447146.6:c.653C= ENSP00000391759.2:p.Ser218=
ENST00000456306.1:c.334C=
ENST00000463529.4:n.999C=
ENST00000465859.2:n.667C=
ENST00000470059.5:n.867C=
ENST00000470062.5:n.625C=
ENST00000473764.5:n.1225C=
ENST00000474671.5:n.713C=
ENST00000477997.5:n.734C=
NM_001032381.1:c.653C= NP_001027553.1:p.Ser218=
NM_001032382.1:c.653C= NP_001027554.1:p.Ser218=
NM_001032383.1:c.653C= NP_001027555.1:p.Ser218=
NM_001032384.1:c.653C= NP_001027556.1:p.Ser218=
NM_001167989.1:c.650C= NP_001161461.1:p.Ser217=
NM_001167990.1:c.629C= NP_001161462.1:p.Ser210=
NM_001167992.1:c.353C= NP_001161464.1:p.Ser118=
NM_005710.2:c.653C= NP_005701.1:p.Ser218=
NM_144495.2:c.368C= NP_652766.1:p.Ser123=
XM_005272571.3:c.650C= XP_005272628.1:p.Ser217=
XM_005272572.3:c.368C= XP_005272629.1:p.Ser123=
XM_011543884.1:c.653C= XP_011542186.1:p.Ser218=
XM_005272572.4:c.368C= XP_005272629.1:p.Ser123=
XM_011543884.2:c.653C= XP_011542186.1:p.Ser218=
XM_017029207.1:c.650C= XP_016884696.1:p.Ser217=
NM_001032381.2:c.653C= NP_001027553.1:p.Ser218=
NM_001032382.2:c.653C= MANE Select NP_001027554.1:p.Ser218=
NM_001032383.2:c.653C= NP_001027555.1:p.Ser218=
NM_001167989.2:c.650C= NP_001161461.1:p.Ser217=
NM_001167990.2:c.629C= NP_001161462.1:p.Ser210=
NM_144495.3:c.368C= NP_652766.1:p.Ser123=