Canonical Allele Identifier: CA412891432

Gene: PQBP1

Linked Data

• MyVariant Identifiers: chrX:g.48760215T>A (hg19) ; chrX:g.48902938T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48902938T>A , CM000685.2:g.48902938T>A	GRCh38
NC_000023.10:g.48760215T>A , CM000685.1:g.48760215T>A	GRCh37
NC_000023.9:g.48645159T>A	NCBI36
NG_015967.1:g.10021T>A
NG_015968.2:g.212A>T
NG_034300.1:g.14021A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218224.9:c.652T>A	ENSP00000218224.4:p.Ser218Thr
ENST00000376563.6:c.652T>A	ENSP00000365747.1:p.Ser218Thr
ENST00000396763.6:c.652T>A	ENSP00000379985.1:p.Ser218Thr
ENST00000443648.6:c.652T>A	ENSP00000414861.2:p.Ser218Thr
ENST00000456306.2:c.43T>A	ENSP00000393013.2:p.Ser15Thr
ENST00000472742.6:c.*69T>A	ENSP00000509191.1:n.*69T>A
ENST00000474671.6:n.1807T>A
ENST00000477997.6:n.1601T>A
ENST00000486150.6:n.1907T>A
ENST00000692023.1:c.*1073T>A	ENSP00000509927.1:n.*1073T>A
ENST00000447146.7:c.652T>A MANE Select	ENSP00000391759.2:p.Ser218Thr
ENST00000651767.1:c.652T>A	ENSP00000498362.1:p.Ser218Thr
ENST00000218224.8:c.652T>A	ENSP00000218224.4:p.Ser218Thr
ENST00000247140.8:c.367T>A	ENSP00000247140.4:p.Ser123Thr
ENST00000376563.5:c.652T>A	ENSP00000365747.1:p.Ser218Thr
ENST00000376566.8:c.367T>A	ENSP00000365750.4:p.Ser123Thr
ENST00000396763.5:c.652T>A	ENSP00000379985.1:p.Ser218Thr
ENST00000447146.6:c.652T>A	ENSP00000391759.2:p.Ser218Thr
ENST00000456306.1:c.333T>A
ENST00000463529.4:n.998T>A
ENST00000465859.2:n.666T>A
ENST00000470059.5:n.866T>A
ENST00000470062.5:n.624T>A
ENST00000473764.5:n.1224T>A
ENST00000474671.5:n.712T>A
ENST00000477997.5:n.733T>A
NM_001032381.1:c.652T>A	NP_001027553.1:p.Ser218Thr
NM_001032382.1:c.652T>A	NP_001027554.1:p.Ser218Thr
NM_001032383.1:c.652T>A	NP_001027555.1:p.Ser218Thr
NM_001032384.1:c.652T>A	NP_001027556.1:p.Ser218Thr
NM_001167989.1:c.649T>A	NP_001161461.1:p.Ser217Thr
NM_001167990.1:c.628T>A	NP_001161462.1:p.Ser210Thr
NM_001167992.1:c.352T>A	NP_001161464.1:p.Ser118Thr
NM_005710.2:c.652T>A	NP_005701.1:p.Ser218Thr
NM_144495.2:c.367T>A	NP_652766.1:p.Ser123Thr
XM_005272571.3:c.649T>A	XP_005272628.1:p.Ser217Thr
XM_005272572.3:c.367T>A	XP_005272629.1:p.Ser123Thr
XM_011543884.1:c.652T>A	XP_011542186.1:p.Ser218Thr
XM_005272572.4:c.367T>A	XP_005272629.1:p.Ser123Thr
XM_011543884.2:c.652T>A	XP_011542186.1:p.Ser218Thr
XM_017029207.1:c.649T>A	XP_016884696.1:p.Ser217Thr
NM_001032381.2:c.652T>A	NP_001027553.1:p.Ser218Thr
NM_001032382.2:c.652T>A MANE Select	NP_001027554.1:p.Ser218Thr
NM_001032383.2:c.652T>A	NP_001027555.1:p.Ser218Thr
NM_001167989.2:c.649T>A	NP_001161461.1:p.Ser217Thr
NM_001167990.2:c.628T>A	NP_001161462.1:p.Ser210Thr
NM_144495.3:c.367T>A	NP_652766.1:p.Ser123Thr