Canonical Allele Identifier: CA412891581

Gene: PQBP1

Linked Data

• MyVariant Identifiers: chrX:g.48760249C>T (hg19) ; chrX:g.48902972C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48902972C>T , CM000685.2:g.48902972C>T	GRCh38
NC_000023.10:g.48760249C>T , CM000685.1:g.48760249C>T	GRCh37
NC_000023.9:g.48645193C>T	NCBI36
NG_015967.1:g.10055C>T
NG_015968.2:g.178G>A
NG_034300.1:g.13987G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218224.9:c.686C>T	ENSP00000218224.4:p.Thr229Ile
ENST00000376563.6:c.686C>T	ENSP00000365747.1:p.Thr229Ile
ENST00000396763.6:c.686C>T	ENSP00000379985.1:p.Thr229Ile
ENST00000443648.6:c.686C>T	ENSP00000414861.2:p.Thr229Ile
ENST00000456306.2:c.77C>T	ENSP00000393013.2:p.Thr26Ile
ENST00000472742.6:c.*103C>T	ENSP00000509191.1:n.*103C>T
ENST00000474671.6:n.1841C>T
ENST00000477997.6:n.1635C>T
ENST00000486150.6:n.1941C>T
ENST00000692023.1:c.*1107C>T	ENSP00000509927.1:n.*1107C>T
ENST00000447146.7:c.686C>T MANE Select	ENSP00000391759.2:p.Thr229Ile
ENST00000651767.1:c.686C>T	ENSP00000498362.1:p.Thr229Ile
ENST00000218224.8:c.686C>T	ENSP00000218224.4:p.Thr229Ile
ENST00000247140.8:c.401C>T	ENSP00000247140.4:p.Thr134Ile
ENST00000376563.5:c.686C>T	ENSP00000365747.1:p.Thr229Ile
ENST00000376566.8:c.401C>T	ENSP00000365750.4:p.Thr134Ile
ENST00000396763.5:c.686C>T	ENSP00000379985.1:p.Thr229Ile
ENST00000447146.6:c.686C>T	ENSP00000391759.2:p.Thr229Ile
ENST00000456306.1:c.367C>T
ENST00000463529.4:n.1032C>T
ENST00000465859.2:n.700C>T
ENST00000470059.5:n.900C>T
ENST00000470062.5:n.658C>T
ENST00000473764.5:n.1258C>T
ENST00000474671.5:n.746C>T
ENST00000477997.5:n.767C>T
NM_001032381.1:c.686C>T	NP_001027553.1:p.Thr229Ile
NM_001032382.1:c.686C>T	NP_001027554.1:p.Thr229Ile
NM_001032383.1:c.686C>T	NP_001027555.1:p.Thr229Ile
NM_001032384.1:c.686C>T	NP_001027556.1:p.Thr229Ile
NM_001167989.1:c.683C>T	NP_001161461.1:p.Thr228Ile
NM_001167990.1:c.662C>T	NP_001161462.1:p.Thr221Ile
NM_001167992.1:c.386C>T	NP_001161464.1:p.Thr129Ile
NM_005710.2:c.686C>T	NP_005701.1:p.Thr229Ile
NM_144495.2:c.401C>T	NP_652766.1:p.Thr134Ile
XM_005272571.3:c.683C>T	XP_005272628.1:p.Thr228Ile
XM_005272572.3:c.401C>T	XP_005272629.1:p.Thr134Ile
XM_011543884.1:c.686C>T	XP_011542186.1:p.Thr229Ile
XM_005272572.4:c.401C>T	XP_005272629.1:p.Thr134Ile
XM_011543884.2:c.686C>T	XP_011542186.1:p.Thr229Ile
XM_017029207.1:c.683C>T	XP_016884696.1:p.Thr228Ile
NM_001032381.2:c.686C>T	NP_001027553.1:p.Thr229Ile
NM_001032382.2:c.686C>T MANE Select	NP_001027554.1:p.Thr229Ile
NM_001032383.2:c.686C>T	NP_001027555.1:p.Thr229Ile
NM_001167989.2:c.683C>T	NP_001161461.1:p.Thr228Ile
NM_001167990.2:c.662C>T	NP_001161462.1:p.Thr221Ile
NM_144495.3:c.401C>T	NP_652766.1:p.Thr134Ile