Canonical Allele Identifier: CA10405957

Gene: PQBP1

Linked Data

• dbSNP Id: rs782726343
• ExAC: X:48759971 G / A
• MyVariant Identifiers: chrX:g.48759971G>A (hg19) ; chrX:g.48902694G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48902694G>A , CM000685.2:g.48902694G>A	GRCh38
NC_000023.10:g.48759971G>A , CM000685.1:g.48759971G>A	GRCh37
NC_000023.9:g.48644915G>A	NCBI36
NG_015967.1:g.9777G>A
NG_015968.2:g.456C>T
NG_034300.1:g.14265C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000218224.9:c.578-38G>A	ENSP00000218224.4:n.578-38G>A
ENST00000376563.6:c.578-38G>A	ENSP00000365747.1:n.578-38G>A
ENST00000396763.6:c.578-38G>A	ENSP00000379985.1:n.578-38G>A
ENST00000443648.6:c.578-38G>A	ENSP00000414861.2:n.578-38G>A
ENST00000456306.2:c.-32-38G>A	ENSP00000393013.2:n.-32-38G>A
ENST00000472742.6:c.445-38G>A	ENSP00000509191.1:n.445-38G>A
ENST00000473764.6:n.1369G>A
ENST00000474671.6:n.1563G>A
ENST00000477997.6:n.1489G>A
ENST00000486150.6:n.1663G>A
ENST00000692023.1:c.*961G>A	ENSP00000509927.1:n.*961G>A
ENST00000447146.7:c.578-38G>A MANE Select	ENSP00000391759.2:n.578-38G>A
ENST00000651767.1:c.578-38G>A	ENSP00000498362.1:n.578-38G>A
ENST00000218224.8:c.578-38G>A	ENSP00000218224.4:n.578-38G>A
ENST00000247140.8:c.293-38G>A	ENSP00000247140.4:n.293-38G>A
ENST00000376563.5:c.578-38G>A	ENSP00000365747.1:n.578-38G>A
ENST00000376566.8:c.293-38G>A	ENSP00000365750.4:n.293-38G>A
ENST00000396763.5:c.578-38G>A	ENSP00000379985.1:n.578-38G>A
ENST00000443648.5:c.578-38G>A	ENSP00000414861.1:n.578-38G>A
ENST00000447146.6:c.578-38G>A	ENSP00000391759.2:n.578-38G>A
ENST00000456306.1:c.259-38G>A
ENST00000463529.4:n.754G>A
ENST00000465859.2:n.592-38G>A
ENST00000470059.5:n.754G>A
ENST00000470062.5:n.550-38G>A
ENST00000472742.5:n.614-38G>A
ENST00000473764.5:n.1150-38G>A
ENST00000474671.5:n.638-38G>A
ENST00000477997.5:n.659-38G>A
NM_001032381.1:c.578-38G>A	NP_001027553.1:n.578-38G>A
NM_001032382.1:c.578-38G>A	NP_001027554.1:n.578-38G>A
NM_001032383.1:c.578-38G>A	NP_001027555.1:n.578-38G>A
NM_001032384.1:c.578-38G>A	NP_001027556.1:n.578-38G>A
NM_001167989.1:c.578-41G>A	NP_001161461.1:n.578-41G>A
NM_001167990.1:c.554-38G>A	NP_001161462.1:n.554-38G>A
NM_001167992.1:c.278-38G>A	NP_001161464.1:n.278-38G>A
NM_005710.2:c.578-38G>A	NP_005701.1:n.578-38G>A
NM_144495.2:c.293-38G>A	NP_652766.1:n.293-38G>A
XM_005272571.3:c.578-41G>A	XP_005272628.1:n.578-41G>A
XM_005272572.3:c.293-38G>A	XP_005272629.1:n.293-38G>A
XM_011543884.1:c.578-38G>A	XP_011542186.1:n.578-38G>A
XM_005272572.4:c.293-38G>A	XP_005272629.1:n.293-38G>A
XM_011543884.2:c.578-38G>A	XP_011542186.1:n.578-38G>A
XM_017029207.1:c.578-41G>A	XP_016884696.1:n.578-41G>A
NM_001032381.2:c.578-38G>A	NP_001027553.1:n.578-38G>A
NM_001032382.2:c.578-38G>A MANE Select	NP_001027554.1:n.578-38G>A
NM_001032383.2:c.578-38G>A	NP_001027555.1:n.578-38G>A
NM_001167989.2:c.578-41G>A	NP_001161461.1:n.578-41G>A
NM_001167990.2:c.554-38G>A	NP_001161462.1:n.554-38G>A
NM_144495.3:c.293-38G>A	NP_652766.1:n.293-38G>A