Canonical Allele Identifier: CA516031514

Gene: PQBP1

Linked Data

• MyVariant Identifiers: chrX:g.48760010A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48902733A>T , CM000685.2:g.48902733A>T	GRCh38
NC_000023.10:g.48760010A>T , CM000685.1:g.48760010A>T	GRCh37
NC_000023.9:g.48644954A>T	NCBI36
NG_015967.1:g.9816A>T
NG_015968.2:g.417T>A
NG_034300.1:g.14226T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000218224.9:c.579A>T	ENSP00000218224.4:p.Ala193=
ENST00000376563.6:c.579A>T	ENSP00000365747.1:p.Ala193=
ENST00000396763.6:c.579A>T	ENSP00000379985.1:p.Ala193=
ENST00000443648.6:c.579A>T	ENSP00000414861.2:p.Ala193=
ENST00000456306.2:c.-31A>T	ENSP00000393013.2:n.-31A>T
ENST00000472742.6:c.446A>T	ENSP00000509191.1:p.Gln149Leu
ENST00000473764.6:n.1408A>T
ENST00000474671.6:n.1602A>T
ENST00000477997.6:n.1528A>T
ENST00000486150.6:n.1702A>T
ENST00000692023.1:c.*1000A>T	ENSP00000509927.1:n.*1000A>T
ENST00000447146.7:c.579A>T MANE Select	ENSP00000391759.2:p.Ala193=
ENST00000651767.1:c.579A>T	ENSP00000498362.1:p.Ala193=
ENST00000218224.8:c.579A>T	ENSP00000218224.4:p.Ala193=
ENST00000247140.8:c.294A>T	ENSP00000247140.4:p.Ala98=
ENST00000376563.5:c.579A>T	ENSP00000365747.1:p.Ala193=
ENST00000376566.8:c.294A>T	ENSP00000365750.4:p.Ala98=
ENST00000396763.5:c.579A>T	ENSP00000379985.1:p.Ala193=
ENST00000443648.5:c.579A>T	ENSP00000414861.1:p.Ala193=
ENST00000447146.6:c.579A>T	ENSP00000391759.2:p.Ala193=
ENST00000456306.1:c.260A>T
ENST00000463529.4:n.793A>T
ENST00000465859.2:n.593A>T
ENST00000470059.5:n.793A>T
ENST00000470062.5:n.551A>T
ENST00000472742.5:n.615A>T
ENST00000473764.5:n.1151A>T
ENST00000474671.5:n.639A>T
ENST00000477997.5:n.660A>T
NM_001032381.1:c.579A>T	NP_001027553.1:p.Ala193=
NM_001032382.1:c.579A>T	NP_001027554.1:p.Ala193=
NM_001032383.1:c.579A>T	NP_001027555.1:p.Ala193=
NM_001032384.1:c.579A>T	NP_001027556.1:p.Ala193=
NM_001167989.1:c.578-2A>T	NP_001161461.1:n.578-2A>T
NM_001167990.1:c.555A>T	NP_001161462.1:p.Ala185=
NM_001167992.1:c.279A>T	NP_001161464.1:p.Ala93=
NM_005710.2:c.579A>T	NP_005701.1:p.Ala193=
NM_144495.2:c.294A>T	NP_652766.1:p.Ala98=
XM_005272571.3:c.578-2A>T	XP_005272628.1:n.578-2A>T
XM_005272572.3:c.294A>T	XP_005272629.1:p.Ala98=
XM_011543884.1:c.579A>T	XP_011542186.1:p.Ala193=
XM_005272572.4:c.294A>T	XP_005272629.1:p.Ala98=
XM_011543884.2:c.579A>T	XP_011542186.1:p.Ala193=
XM_017029207.1:c.578-2A>T	XP_016884696.1:n.578-2A>T
NM_001032381.2:c.579A>T	NP_001027553.1:p.Ala193=
NM_001032382.2:c.579A>T MANE Select	NP_001027554.1:p.Ala193=
NM_001032383.2:c.579A>T	NP_001027555.1:p.Ala193=
NM_001167989.2:c.578-2A>T	NP_001161461.1:n.578-2A>T
NM_001167990.2:c.555A>T	NP_001161462.1:p.Ala185=
NM_144495.3:c.294A>T	NP_652766.1:p.Ala98=