Canonical Allele Identifier: CA2693662909

Gene: PQBP1

Linked Data

• gnomAD v4: X-48902719-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48902719G>C , CM000685.2:g.48902719G>C	GRCh38
NC_000023.10:g.48759996G>C , CM000685.1:g.48759996G>C	GRCh37
NC_000023.9:g.48644940G>C	NCBI36
NG_015967.1:g.9802G>C
NG_015968.2:g.431C>G
NG_034300.1:g.14240C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000218224.9:c.578-13G>C	ENSP00000218224.4:n.578-13G>C
ENST00000376563.6:c.578-13G>C	ENSP00000365747.1:n.578-13G>C
ENST00000396763.6:c.578-13G>C	ENSP00000379985.1:n.578-13G>C
ENST00000443648.6:c.578-13G>C	ENSP00000414861.2:n.578-13G>C
ENST00000456306.2:c.-32-13G>C	ENSP00000393013.2:n.-32-13G>C
ENST00000472742.6:c.445-13G>C	ENSP00000509191.1:n.445-13G>C
ENST00000473764.6:n.1394G>C
ENST00000474671.6:n.1588G>C
ENST00000477997.6:n.1514G>C
ENST00000486150.6:n.1688G>C
ENST00000692023.1:c.*986G>C	ENSP00000509927.1:n.*986G>C
ENST00000447146.7:c.578-13G>C MANE Select	ENSP00000391759.2:n.578-13G>C
ENST00000651767.1:c.578-13G>C	ENSP00000498362.1:n.578-13G>C
ENST00000218224.8:c.578-13G>C	ENSP00000218224.4:n.578-13G>C
ENST00000247140.8:c.293-13G>C	ENSP00000247140.4:n.293-13G>C
ENST00000376563.5:c.578-13G>C	ENSP00000365747.1:n.578-13G>C
ENST00000376566.8:c.293-13G>C	ENSP00000365750.4:n.293-13G>C
ENST00000396763.5:c.578-13G>C	ENSP00000379985.1:n.578-13G>C
ENST00000443648.5:c.578-13G>C	ENSP00000414861.1:n.578-13G>C
ENST00000447146.6:c.578-13G>C	ENSP00000391759.2:n.578-13G>C
ENST00000456306.1:c.259-13G>C
ENST00000463529.4:n.779G>C
ENST00000465859.2:n.592-13G>C
ENST00000470059.5:n.779G>C
ENST00000470062.5:n.550-13G>C
ENST00000472742.5:n.614-13G>C
ENST00000473764.5:n.1150-13G>C
ENST00000474671.5:n.638-13G>C
ENST00000477997.5:n.659-13G>C
NM_001032381.1:c.578-13G>C	NP_001027553.1:n.578-13G>C
NM_001032382.1:c.578-13G>C	NP_001027554.1:n.578-13G>C
NM_001032383.1:c.578-13G>C	NP_001027555.1:n.578-13G>C
NM_001032384.1:c.578-13G>C	NP_001027556.1:n.578-13G>C
NM_001167989.1:c.578-16G>C	NP_001161461.1:n.578-16G>C
NM_001167990.1:c.554-13G>C	NP_001161462.1:n.554-13G>C
NM_001167992.1:c.278-13G>C	NP_001161464.1:n.278-13G>C
NM_005710.2:c.578-13G>C	NP_005701.1:n.578-13G>C
NM_144495.2:c.293-13G>C	NP_652766.1:n.293-13G>C
XM_005272571.3:c.578-16G>C	XP_005272628.1:n.578-16G>C
XM_005272572.3:c.293-13G>C	XP_005272629.1:n.293-13G>C
XM_011543884.1:c.578-13G>C	XP_011542186.1:n.578-13G>C
XM_005272572.4:c.293-13G>C	XP_005272629.1:n.293-13G>C
XM_011543884.2:c.578-13G>C	XP_011542186.1:n.578-13G>C
XM_017029207.1:c.578-16G>C	XP_016884696.1:n.578-16G>C
NM_001032381.2:c.578-13G>C	NP_001027553.1:n.578-13G>C
NM_001032382.2:c.578-13G>C MANE Select	NP_001027554.1:n.578-13G>C
NM_001032383.2:c.578-13G>C	NP_001027555.1:n.578-13G>C
NM_001167989.2:c.578-16G>C	NP_001161461.1:n.578-16G>C
NM_001167990.2:c.554-13G>C	NP_001161462.1:n.554-13G>C
NM_144495.3:c.293-13G>C	NP_652766.1:n.293-13G>C