Canonical Allele Identifier: CA516359807

Gene: PQBP1

Linked Data

• MyVariant Identifiers: chrX:g.48759760G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48902483G>T , CM000685.2:g.48902483G>T	GRCh38
NC_000023.10:g.48759760G>T , CM000685.1:g.48759760G>T	GRCh37
NC_000023.9:g.48644704G>T	NCBI36
NG_015967.1:g.9566G>T
NG_015968.2:g.667C>A
NG_034300.1:g.14476C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218224.9:c.543G>T	ENSP00000218224.4:p.Arg181=
ENST00000376563.6:c.543G>T	ENSP00000365747.1:p.Arg181=
ENST00000396763.6:c.543G>T	ENSP00000379985.1:p.Arg181=
ENST00000443648.6:c.543G>T	ENSP00000414861.2:p.Arg181=
ENST00000456306.2:c.-32-249G>T	ENSP00000393013.2:n.-32-249G>T
ENST00000472742.6:c.444+99G>T	ENSP00000509191.1:n.444+99G>T
ENST00000473764.6:n.1158G>T
ENST00000474671.6:n.1352G>T
ENST00000477997.6:n.1278G>T
ENST00000486150.6:n.1452G>T
ENST00000692023.1:c.*750G>T	ENSP00000509927.1:n.*750G>T
ENST00000447146.7:c.543G>T MANE Select	ENSP00000391759.2:p.Arg181=
ENST00000651767.1:c.543G>T	ENSP00000498362.1:p.Arg181=
ENST00000218224.8:c.543G>T	ENSP00000218224.4:p.Arg181=
ENST00000247140.8:c.293-249G>T	ENSP00000247140.4:n.293-249G>T
ENST00000376563.5:c.543G>T	ENSP00000365747.1:p.Arg181=
ENST00000376566.8:c.293-249G>T	ENSP00000365750.4:n.293-249G>T
ENST00000396763.5:c.543G>T	ENSP00000379985.1:p.Arg181=
ENST00000443648.5:c.543G>T	ENSP00000414861.1:p.Arg181=
ENST00000447146.6:c.543G>T	ENSP00000391759.2:p.Arg181=
ENST00000456306.1:c.259-249G>T
ENST00000463529.4:n.543G>T
ENST00000465859.2:n.557G>T
ENST00000470059.5:n.543G>T
ENST00000470062.5:n.549+99G>T
ENST00000472742.5:n.613+99G>T
ENST00000473764.5:n.1115G>T
ENST00000474671.5:n.603G>T
ENST00000477997.5:n.624G>T
NM_001032381.1:c.543G>T	NP_001027553.1:p.Arg181=
NM_001032382.1:c.543G>T	NP_001027554.1:p.Arg181=
NM_001032383.1:c.543G>T	NP_001027555.1:p.Arg181=
NM_001032384.1:c.543G>T	NP_001027556.1:p.Arg181=
NM_001167989.1:c.543G>T	NP_001161461.1:p.Arg181=
NM_001167990.1:c.519G>T	NP_001161462.1:p.Arg173=
NM_001167992.1:c.243G>T	NP_001161464.1:p.Arg81=
NM_005710.2:c.543G>T	NP_005701.1:p.Arg181=
NM_144495.2:c.293-249G>T	NP_652766.1:n.293-249G>T
XM_005272571.3:c.543G>T	XP_005272628.1:p.Arg181=
XM_005272572.3:c.293-249G>T	XP_005272629.1:n.293-249G>T
XM_011543884.1:c.543G>T	XP_011542186.1:p.Arg181=
XM_005272572.4:c.293-249G>T	XP_005272629.1:n.293-249G>T
XM_011543884.2:c.543G>T	XP_011542186.1:p.Arg181=
XM_017029207.1:c.543G>T	XP_016884696.1:p.Arg181=
NM_001032381.2:c.543G>T	NP_001027553.1:p.Arg181=
NM_001032382.2:c.543G>T MANE Select	NP_001027554.1:p.Arg181=
NM_001032383.2:c.543G>T	NP_001027555.1:p.Arg181=
NM_001167989.2:c.543G>T	NP_001161461.1:p.Arg181=
NM_001167990.2:c.519G>T	NP_001161462.1:p.Arg173=
NM_144495.3:c.293-249G>T	NP_652766.1:n.293-249G>T