Canonical Allele Identifier: CA516031584

Gene: PQBP1

Linked Data

• gnomAD v4: X-48902794-C-A
• MyVariant Identifiers: chrX:g.48760071C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48902794C>A , CM000685.2:g.48902794C>A	GRCh38
NC_000023.10:g.48760071C>A , CM000685.1:g.48760071C>A	GRCh37
NC_000023.9:g.48645015C>A	NCBI36
NG_015967.1:g.9877C>A
NG_015968.2:g.356G>T
NG_034300.1:g.14165G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218224.9:c.640C>A	ENSP00000218224.4:p.Arg214=
ENST00000376563.6:c.640C>A	ENSP00000365747.1:p.Arg214=
ENST00000396763.6:c.640C>A	ENSP00000379985.1:p.Arg214=
ENST00000443648.6:c.640C>A	ENSP00000414861.2:p.Arg214=
ENST00000456306.2:c.31C>A	ENSP00000393013.2:p.Arg11=
ENST00000472742.6:c.*57C>A	ENSP00000509191.1:n.*57C>A
ENST00000473764.6:n.1469C>A
ENST00000474671.6:n.1663C>A
ENST00000477997.6:n.1589C>A
ENST00000486150.6:n.1763C>A
ENST00000692023.1:c.*1061C>A	ENSP00000509927.1:n.*1061C>A
ENST00000447146.7:c.640C>A MANE Select	ENSP00000391759.2:p.Arg214=
ENST00000651767.1:c.640C>A	ENSP00000498362.1:p.Arg214=
ENST00000218224.8:c.640C>A	ENSP00000218224.4:p.Arg214=
ENST00000247140.8:c.355C>A	ENSP00000247140.4:p.Arg119=
ENST00000376563.5:c.640C>A	ENSP00000365747.1:p.Arg214=
ENST00000376566.8:c.355C>A	ENSP00000365750.4:p.Arg119=
ENST00000396763.5:c.640C>A	ENSP00000379985.1:p.Arg214=
ENST00000447146.6:c.640C>A	ENSP00000391759.2:p.Arg214=
ENST00000456306.1:c.321C>A
ENST00000463529.4:n.854C>A
ENST00000465859.2:n.654C>A
ENST00000470059.5:n.854C>A
ENST00000470062.5:n.612C>A
ENST00000473764.5:n.1212C>A
ENST00000474671.5:n.700C>A
ENST00000477997.5:n.721C>A
NM_001032381.1:c.640C>A	NP_001027553.1:p.Arg214=
NM_001032382.1:c.640C>A	NP_001027554.1:p.Arg214=
NM_001032383.1:c.640C>A	NP_001027555.1:p.Arg214=
NM_001032384.1:c.640C>A	NP_001027556.1:p.Arg214=
NM_001167989.1:c.637C>A	NP_001161461.1:p.Arg213=
NM_001167990.1:c.616C>A	NP_001161462.1:p.Arg206=
NM_001167992.1:c.340C>A	NP_001161464.1:p.Arg114=
NM_005710.2:c.640C>A	NP_005701.1:p.Arg214=
NM_144495.2:c.355C>A	NP_652766.1:p.Arg119=
XM_005272571.3:c.637C>A	XP_005272628.1:p.Arg213=
XM_005272572.3:c.355C>A	XP_005272629.1:p.Arg119=
XM_011543884.1:c.640C>A	XP_011542186.1:p.Arg214=
XM_005272572.4:c.355C>A	XP_005272629.1:p.Arg119=
XM_011543884.2:c.640C>A	XP_011542186.1:p.Arg214=
XM_017029207.1:c.637C>A	XP_016884696.1:p.Arg213=
NM_001032381.2:c.640C>A	NP_001027553.1:p.Arg214=
NM_001032382.2:c.640C>A MANE Select	NP_001027554.1:p.Arg214=
NM_001032383.2:c.640C>A	NP_001027555.1:p.Arg214=
NM_001167989.2:c.637C>A	NP_001161461.1:p.Arg213=
NM_001167990.2:c.616C>A	NP_001161462.1:p.Arg206=
NM_144495.3:c.355C>A	NP_652766.1:p.Arg119=