Canonical Allele Identifier: CA2428428045
Gene: PQBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48902776T= , CM000685.2:g.48902776T= GRCh38
NC_000023.10:g.48760053T= , CM000685.1:g.48760053T= GRCh37
NC_000023.9:g.48644997T= NCBI36
NG_015967.1:g.9859T=
NG_015968.2:g.374A=
NG_034300.1:g.14183A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000218224.9:c.622T= ENSP00000218224.4:p.Ser208=
ENST00000376563.6:c.622T= ENSP00000365747.1:p.Ser208=
ENST00000396763.6:c.622T= ENSP00000379985.1:p.Ser208=
ENST00000443648.6:c.622T= ENSP00000414861.2:p.Ser208=
ENST00000456306.2:c.13T= ENSP00000393013.2:p.Ser5=
ENST00000472742.6:c.*39T= ENSP00000509191.1:n.*39T=
ENST00000473764.6:n.1451T=
ENST00000474671.6:n.1645T=
ENST00000477997.6:n.1571T=
ENST00000486150.6:n.1745T=
ENST00000692023.1:c.*1043T= ENSP00000509927.1:n.*1043T=
ENST00000447146.7:c.622T= MANE Select ENSP00000391759.2:p.Ser208=
ENST00000651767.1:c.622T= ENSP00000498362.1:p.Ser208=
ENST00000218224.8:c.622T= ENSP00000218224.4:p.Ser208=
ENST00000247140.8:c.337T= ENSP00000247140.4:p.Ser113=
ENST00000376563.5:c.622T= ENSP00000365747.1:p.Ser208=
ENST00000376566.8:c.337T= ENSP00000365750.4:p.Ser113=
ENST00000396763.5:c.622T= ENSP00000379985.1:p.Ser208=
ENST00000443648.5:c.622T= ENSP00000414861.1:p.Ser208=
ENST00000447146.6:c.622T= ENSP00000391759.2:p.Ser208=
ENST00000456306.1:c.303T=
ENST00000463529.4:n.836T=
ENST00000465859.2:n.636T=
ENST00000470059.5:n.836T=
ENST00000470062.5:n.594T=
ENST00000472742.5:n.658T=
ENST00000473764.5:n.1194T=
ENST00000474671.5:n.682T=
ENST00000477997.5:n.703T=
NM_001032381.1:c.622T= NP_001027553.1:p.Ser208=
NM_001032382.1:c.622T= NP_001027554.1:p.Ser208=
NM_001032383.1:c.622T= NP_001027555.1:p.Ser208=
NM_001032384.1:c.622T= NP_001027556.1:p.Ser208=
NM_001167989.1:c.619T= NP_001161461.1:p.Ser207=
NM_001167990.1:c.598T= NP_001161462.1:p.Ser200=
NM_001167992.1:c.322T= NP_001161464.1:p.Ser108=
NM_005710.2:c.622T= NP_005701.1:p.Ser208=
NM_144495.2:c.337T= NP_652766.1:p.Ser113=
XM_005272571.3:c.619T= XP_005272628.1:p.Ser207=
XM_005272572.3:c.337T= XP_005272629.1:p.Ser113=
XM_011543884.1:c.622T= XP_011542186.1:p.Ser208=
XM_005272572.4:c.337T= XP_005272629.1:p.Ser113=
XM_011543884.2:c.622T= XP_011542186.1:p.Ser208=
XM_017029207.1:c.619T= XP_016884696.1:p.Ser207=
NM_001032381.2:c.622T= NP_001027553.1:p.Ser208=
NM_001032382.2:c.622T= MANE Select NP_001027554.1:p.Ser208=
NM_001032383.2:c.622T= NP_001027555.1:p.Ser208=
NM_001167989.2:c.619T= NP_001161461.1:p.Ser207=
NM_001167990.2:c.598T= NP_001161462.1:p.Ser200=
NM_144495.3:c.337T= NP_652766.1:p.Ser113=