Canonical Allele Identifier: CA412891535
Gene: PQBP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48902962G>A , CM000685.2:g.48902962G>A GRCh38
NC_000023.10:g.48760239G>A , CM000685.1:g.48760239G>A GRCh37
NC_000023.9:g.48645183G>A NCBI36
NG_015967.1:g.10045G>A
NG_015968.2:g.188C>T
NG_034300.1:g.13997C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000218224.9:c.676G>A ENSP00000218224.4:p.Glu226Lys
ENST00000376563.6:c.676G>A ENSP00000365747.1:p.Glu226Lys
ENST00000396763.6:c.676G>A ENSP00000379985.1:p.Glu226Lys
ENST00000443648.6:c.676G>A ENSP00000414861.2:p.Glu226Lys
ENST00000456306.2:c.67G>A ENSP00000393013.2:p.Glu23Lys
ENST00000472742.6:c.*93G>A ENSP00000509191.1:n.*93G>A
ENST00000474671.6:n.1831G>A
ENST00000477997.6:n.1625G>A
ENST00000486150.6:n.1931G>A
ENST00000692023.1:c.*1097G>A ENSP00000509927.1:n.*1097G>A
ENST00000447146.7:c.676G>A MANE Select ENSP00000391759.2:p.Glu226Lys
ENST00000651767.1:c.676G>A ENSP00000498362.1:p.Glu226Lys
ENST00000218224.8:c.676G>A ENSP00000218224.4:p.Glu226Lys
ENST00000247140.8:c.391G>A ENSP00000247140.4:p.Glu131Lys
ENST00000376563.5:c.676G>A ENSP00000365747.1:p.Glu226Lys
ENST00000376566.8:c.391G>A ENSP00000365750.4:p.Glu131Lys
ENST00000396763.5:c.676G>A ENSP00000379985.1:p.Glu226Lys
ENST00000447146.6:c.676G>A ENSP00000391759.2:p.Glu226Lys
ENST00000456306.1:c.357G>A
ENST00000463529.4:n.1022G>A
ENST00000465859.2:n.690G>A
ENST00000470059.5:n.890G>A
ENST00000470062.5:n.648G>A
ENST00000473764.5:n.1248G>A
ENST00000474671.5:n.736G>A
ENST00000477997.5:n.757G>A
NM_001032381.1:c.676G>A NP_001027553.1:p.Glu226Lys
NM_001032382.1:c.676G>A NP_001027554.1:p.Glu226Lys
NM_001032383.1:c.676G>A NP_001027555.1:p.Glu226Lys
NM_001032384.1:c.676G>A NP_001027556.1:p.Glu226Lys
NM_001167989.1:c.673G>A NP_001161461.1:p.Glu225Lys
NM_001167990.1:c.652G>A NP_001161462.1:p.Glu218Lys
NM_001167992.1:c.376G>A NP_001161464.1:p.Glu126Lys
NM_005710.2:c.676G>A NP_005701.1:p.Glu226Lys
NM_144495.2:c.391G>A NP_652766.1:p.Glu131Lys
XM_005272571.3:c.673G>A XP_005272628.1:p.Glu225Lys
XM_005272572.3:c.391G>A XP_005272629.1:p.Glu131Lys
XM_011543884.1:c.676G>A XP_011542186.1:p.Glu226Lys
XM_005272572.4:c.391G>A XP_005272629.1:p.Glu131Lys
XM_011543884.2:c.676G>A XP_011542186.1:p.Glu226Lys
XM_017029207.1:c.673G>A XP_016884696.1:p.Glu225Lys
NM_001032381.2:c.676G>A NP_001027553.1:p.Glu226Lys
NM_001032382.2:c.676G>A MANE Select NP_001027554.1:p.Glu226Lys
NM_001032383.2:c.676G>A NP_001027555.1:p.Glu226Lys
NM_001167989.2:c.673G>A NP_001161461.1:p.Glu225Lys
NM_001167990.2:c.652G>A NP_001161462.1:p.Glu218Lys
NM_144495.3:c.391G>A NP_652766.1:p.Glu131Lys